疾病名称 |
别名 |
|
Myopathy, Myofibrillar, 1 |
Desmin-Related Myofibrillar Myopathy
|
Desmin-Related Myopathy
|
MFM1
|
Myopathy, Myofibrillar, Desmin-Related
|
Drm
|
Myofibrillar Myopathy With Arrhythmogenic Right Ventricular Cardiomyopathy
|
Desmin-Related Myopathy With Arrhythmogenic Right Ventricular Cardiomyopathy
|
Myofibrillar Myopathy 1
|
Desminopathy
|
Muscular Dystrophy, Limb-Girdle, Type 2r
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 7
|
Desminopathy, Primary
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 7, Formerly
|
Arvd7, Formerly
|
Arrhythmogenic Right Ventricular Cardiomyopathy 7, Formerly
|
Arvc7, Formerly
|
Inclusion Body Myopathy 1, Autosomal Dominant, Formerly
|
Ibm1, Formerly
|
Cardiomyopathy, Dilated, 1f And Limb-Girdle Muscular Dystrophy Type 1d, Formerly
|
Cmd1f And Lgmd1d, Formerly
|
Cardiomyopathy, Dilated, With Conduction Defect And Muscular Dystrophy
|
Cdcd3, Formerly
|
Muscular Dystrophy, Limb-Girdle, Type 2r, Formerly
|
Lgmd2r, Formerly
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2r
|
Arrhythmogenic Right Ventricular Cardiomyopathy 7
|
Arvc7
|
Arvd7
|
Autosomal Dominant Inclusion Body Myopathy 1
|
Cdcd3
|
Cmd1f And Lgmd1d
|
Desminopathy Primary
|
Dilated Cardiomyopathy 1f And Limb-Girdle Muscular Dystrophy Type 1d
|
Dilated Cardiomyopathy With Conduction Defect And Muscular Dystrophy
|
Familial Arrhythmogenic Right Ventricular Dysplasia 7
|
Lgmd2r
|
Limb-Girdle Muscular Dystrophy 2r
|
Mfm Desmin-Related
|
Myopathy Myofibrillar Desmin-Related
|
Dystrophy, Muscular, Limb-Girdle, Type 2r
|
|
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type |
KAESER SYNDROME
|
Stark-Kaeser Syndrome
|
Neurogenic Scapuloperoneal Syndrome Kaeser Type
|
Neurogenic Scapuloperoneal Syndrome, Kaeser Type
|
Scapuloperoneal Syndrome, Neurogenic Type, Of Kaeser
|
SCPNK
|
Scapuloperoneal Syndrome Type Kaeser
|
|
|
Cardiomyopathy, Dilated, 1i |
CMD1I
|
Dilated Cardiomyopathy 1i
|
Cardiomyopathy, Dilated 1i
|
Cardiomyopathy, Dilated, Type 1i
|
|
|
Myofibrillar Myopathy |
Desmin Related Myopathy
|
Myotilinopathy
|
Myopathy, Myofibrillar
|
Alpha Beta Crystallinopathy
|
Desmin Storage Myopathy
|
Desminopathy
|
Filaminopathy
|
Protein Surplus Myopathy
|
Zaspopathy
|
Myofibrillar Myopathies
|
Myopathy, Myofibrillar, Desmin-Related
|
Myopathy, Desmin Storage
|
Mfm - [Myofibrillar Myopathy]
|
|
|
Dilated Cardiomyopathy |
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
Cardiomyopathy, Dilated
|
DCM
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
Cardiomyopathy, Dilated, 1e |
Left Ventricular Noncompaction 9
|
Left Ventricular Noncompaction 5
|
Dilated Cardiomyopathy 1e
|
Dilated Cardiomyopathy 1s
|
CMD1E
|
Cdcd2
|
Cardiomyopathy, Dilated, 1y
|
CMD1Y
|
Cardiomyopathy, Dilated, 1s
|
CMD1S
|
Dilated Cardiomyopathy 1y
|
Dilated Cardiomyopathy With Conduction Defect 2
|
Dilated Cardiomyopathy With Conduction Disorder And Arrhythmia
|
Cardiomyopathy, Dilated, With Conduction Disorder And Arrhythmia
|
Cardiomyopathy, Dilated, With Conduction Defect 2
|
Cardiomyopathy Dilated With Conduction Defect Type 2
|
Cardiomyopathy, Dilated 1e
|
Cardiomyopathy, Dilated 1s
|
Cardiomyopathy, Dilated 1y
|
Left Ventricular Non-Compaction 5
|
LVNC5
|
Left Ventricular Non-Compaction 9
|
LVNC9
|
Cardiomyopathy, Dilated, Type 1e
|
Cardiomyopathy, Dilated, Type 1s
|
Cardiomyopathy, Dilated, Type 1y
|
|
|
Arrhythmogenic Right Ventricular Cardiomyopathy |
Arrhythmogenic Right Ventricular Dysplasia
|
Arvc
|
Arvd
|
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
|
Arvc Cardiomyopathy
|
Arrhythmogenic Right Ventricular Cardiomyopathy-Dysplasia
|
Arvd/C
|
Right Ventricular Dysplasia, Arrhythmogenic
|
Ventricular Dysplasia, Right, Arrhythmogenic
|
Cardiomyopathy, Ventricular, Right, Arrhythmogenic
|
Dysplasia, Arrhythmogenic Right Ventricular
|
|
|
Familial Isolated Dilated Cardiomyopathy |
Familial Or Idiopathic Dilated Cardiomyopathy
|
|
|
Progressive Familial Heart Block |
Hereditary Bundle Branch Defect
|
Hereditary Bundle Branch System Defect
|
Familial Lenegre Disease
|
Familial Lev Disease
|
Familial Lev-Lenegre Disease
|
Familial Pccd
|
Familial Progressive Heart Block
|
Pfhb
|
Bundle Branch Block
|
Hbbd
|
Lenegre Lev Disease
|
Lev Syndrome
|
Lev'S Disease
|
Lev-Lenègre Disease
|
Pccd
|
Progressive Cardiac Conduction Defect
|
Bundle-Branch Block
|
|
|
Progressive Familial Heart Block, Type Ia |
PFHB1A
|
Bundle Branch Block
|
Heart Block, Nonprogressive
|
Lenegre-Lev Disease
|
Hereditary Bundle Branch System Defect
|
Progressive Familial Heart Block Type Ia
|
Pfhbia
|
Pccd
|
Hbbd
|
Progressive Familial Heart Block, Type 1a
|
Heart Block, Progressive Familial, Type I
|
Pfhbi
|
Cardiac Conduction Defect, Progressive
|
Heart Block, Progressive, Type Ia
|
Progressive Familial Heart Block Type 1a
|
Familial Progressive Cardiac Conduction Defect
|
Heart Block Progressive Familial Type 1
|
Familial Lenègre Disease
|
Familial Lev Disease
|
Familial Lev-Lenègre Disease
|
Familial Pccd
|
Familial Progressive Heart Block
|
Hereditary Bundle Branch Defect
|
Progressive Familial Heart Block
|
Progressive Familial Heart Block 1a
|
Cardiac Conduction Defect
|
Progressive Cardiac Conduction Defect
|
Progressive Familial Heart Block Type I
|
Heart Block, Progressive, Familial, Type 1a
|
Bundle-Branch Block
|
Conduction Disorder Of The Heart
|
|
|
Lymphangioleiomyomatosis |
Lymphangiomyomatosis
|
LAM
|
Lung Lymphangioleiomyomatosis
|
Pulmonary Lymphangioleiomyomatosis
|
Lymphangioleiomyomatosis, Somatic
|
Lymphangio-Myomatosis
|
|
|
Neuromuscular Disease |
Neuromuscular Diseases
|
Neuromuscular Disorders
|
Neuromuscular Disorder
|
|
|
Mesenchymal Chondrosarcoma |
Chondrosarcoma, Mesenchymal
|
Chondrosarcoma Mesenchymal
|
|
|
Epithelioid Leiomyosarcoma |
Leiomyosarcoma Epithelioid
|
Leiomyosarcoma, Epithelioid
|
|
|
Adenosarcoma |
|
|
Cardioneuromyopathy With Hyaline Masses And Nemaline Rods |
|
|
Restrictive Cardiomyopathy |
Familial Restrictive Cardiomyopathy
|
Cardiomyopathy, Restrictive
|
Cardiomyopathy, Constrictive
|
Primary Restrictive Cardiomyopathy
|
Rcm
|
Cardiomyopathy Restrictive
|
|
|
Dedifferentiated Liposarcoma |
Ddls
|
Liposarcoma Dedifferentiated
|
Liposarcoma, Dedifferentiated
|
|
|
Fibromatosis |
|
|
Glomus Tumor |
Glomus Neoplasm
|
Glomus Tumour
|
|
|
Myopathy |
Muscular Diseases
|
Myopathies
|
|
|
Alveolar Soft Part Sarcoma |
ASPS
|
Alveolar Soft-Part Sarcoma
|
Sarcoma, Alveolar Soft Part
|
Alveolar Soft Tissue Sarcoma
|
Sarcoma Alveolar Soft Part
|
Adult Alveolar Soft-Part Sarcoma
|
Childhood Alveolar Soft-Part Sarcoma
|
|
|
Leiomyosarcoma |
|
|
Fibroma |
|
|
Carcinosarcoma |
Mixed Tumor, Mullerian
|
Malignant Mixed Mesodermal Tumor
|
Malignant Mixed Mullerian Tumor
|
Mmmt
|
Mixed Tumor, Mesodermal
|
Mesodermal Mixed Tumor
|
Mixed Mesodermal Tumor
|
Mullerian Mixed Tumor
|
Mixed Mullerian Tumor
|
Malignant Mixed Müllerian Tumor
|
Mixed Müllerian Tumor
|
Mixed Tumor Mullerian
|
Mixed Tumor, Not Otherwise Specified
|
|
|
Fibrous Histiocytoma |
Benign Fibrous Histiocytoma
|
Histiocytoma, Benign Fibrous
|
Fibroxanthoma
|
Histiocytoma Fibrous
|
|
|
Embryonal Rhabdomyosarcoma |
Rhabdomyosarcoma, Embryonal
|
Rhabdomyosarcoma Embryonal
|
Botryoid Rhabdomyosarcoma
|
Erms
|
Spindle Cell Rhabdomyosarcomas
|
|
|
Granular Cell Tumor |
Abrikosov'S Tumor
|
Neoplasm Of Granular Cell
|
Abrikosoff'S Granulous Cell Tumor
|
Abrikosoff'S Tumor
|
Giant Granulocellular Abrikosov'S Tumor
|
Malignant Variant Of Abrikosov'S Tumor
|
Carcinoma, Granular Cell
|
|
|
Myopathy, Spheroid Body |
Spheroid Body Myopathy
|
Autosomal Dominant Spheroid Body Myopathy
|
SBM
|
|
|
Medullary Colon Carcinoma |
|
|
Angiomyolipoma |
|
|
Endometrial Stromal Sarcoma |
Ess
|
Endometrial Stromal Sarcoma, High Grade
|
Undifferentiated Endometrial Sarcoma
|
Stromal Sarcoma Of The Corpus Uteri
|
Sarcoma Endometrial Stromal
|
Sarcoma, Endometrial Stromal
|
Undifferentiated Stromal Sarcoma
|
|
|
Dermatofibrosarcoma Protuberans |
DFSP
|
Dermatofibrosarcoma
|
Giant Cell Fibroblastoma
|
Metastatic Dermatofibrosarcoma Protuberans
|
Familial Dermatofibrosarcoma Protuberans
|
Darier-Ferrand Tumor
|
Darier-Hoffmann Tumor
|
|
|
Desmoplastic Small Round Cell Tumor |
Dsrct
|
Desmoplastic Small Round-Cell Tumor
|
Desmoplastic Small Round-Cell Neoplasm
|
|
|
Miyoshi Muscular Dystrophy |
Distal Myopathy
|
Distal Muscular Dystrophy
|
Miyoshi Myopathy
|
Distal Myopathies
|
Dystrophy, Muscular, Miyoshi
|
Myopathy, Distal
|
Distal Muscular Dystrophies
|
|
|
Leiomyoma |
Leiomyomatous Neoplasm
|
Leiomyomatous Tumor
|
Leiomyomas
|
Fibroid Tumor
|
Uterine Fibroids
|
|
|
Malignant Fibrous Histiocytoma |
Undifferentiated Pleomorphic Sarcoma
|
Ups
|
Histiocytoma, Malignant Fibrous
|
Fibroxanthosarcoma
|
Mfh
|
Malignant Fibrohistiocytic Tumors
|
Histiocytoma, Fibrous, Malignant
|
|
|
Infantile Myofibromatosis |
Lipofibromatosis
|
Myofibromatosis
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 |
Asymmetric Septal Hypertrophy
|
Familial Hypertrophic Cardiomyopathy
|
Hypertrophic Cardiomyopathy 1
|
CMH1
|
Hypertrophic Cardiomyopathy 19
|
CMH
|
Ventricular Hypertrophy, Hereditary
|
Ash
|
Hypertrophic Subaortic Stenosis, Idiopathic
|
Cardiomyopathy, Familial Hypertrophic
|
Cardiomyopathy, Hypertrophic, 1, Digenic
|
Cardiomyopathy, Familial Hypertrophic 1
|
Hcm
|
Hereditary Ventricular Hypertrophy
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Hypertrophic Cardiomyopathy
|
Cardiomyopathy, Hypertrophic, Familial
|
Cardiomyopathy, Hypertrophic, 1
|
Familial Asymmetric Septal Hypertrophy
|
Heritable Hypertrophic Cardiomyopathy
|
Fhc
|
Cardiomyopathy, Hypertrophic, Familial, Type 1
|
|
|
Liposarcoma |
|
|
Gastrointestinal Stromal Tumor |
GIST
|
Gastrointestinal Stromal Tumors
|
Gastrointestinal Stromal Sarcoma
|
Gastrointestinal Stromal Tumor, Familial
|
Gant
|
Gastrointestinal Stromal Tumour
|
Stromal Tumor Of Gastrointestinal Tract
|
Stromal Tumour Of Gastrointestinal Tract
|
Gastrointestinal Stromal Neoplasm
|
Paraganglioma And Gastric Stromal Sarcoma
|
Plexosarcoma
|
|
|
Muscle Cancer |
Myosarcoma
|
Malignant Neoplasm Of Muscle
|
Malignant Tumor Of Muscle
|
Malignant Tumor Of The Muscle
|
Muscle Neoplasms
|
Myomatous Neoplasm
|
|
|
Angiolipoma |
|
|
Uterus Leiomyosarcoma |
Leiomyosarcoma Of Uterus
|
Leiomyosarcoma Of Corpus Uteri
|
Leiomyosarcoma Of The Corpus Uteri
|
Uterine Leiomyosarcoma
|
|
|
Uterine Sarcoma |
Sarcoma Of The Uterus
|
Uterine Corpus Sarcoma
|
|
|
Pseudosarcomatous Fibromatosis |
Nodular Fasciitis
|
Pseudosarcomatous Fasciitis
|
Fasciitis - Nodular
|
Fasciitis Nodular
|
|
|
Smooth Muscle Tumor |
|
|
Pleomorphic Adenoma |
Mixed Tumor Of The Salivary Gland
|
Adenoma Pleomorphic
|
Adenoma, Pleomorphic
|
Mixed Salivary Gland Tumor
|
Mixed Tumor, Not Otherwise Specified
|
|
|
Spindle Cell Sarcoma |
Sarcoma
|
Sarcoma Spindle Cell
|
Sarcoma, Spindle Cell
|
Sarcoma - Category
|
|
|
Atrioventricular Block |
|
|
Hemangiopericytoma, Malignant |
Hemangiopericytoma
|
Haemangiopericytic Meningioma
|
Malignant Hemangiopericytoma
|
Solitary Fibrous Tumor
|
|
|
Centronuclear Myopathy |
Myopathy, Centronuclear
|
Myotubular Myopathy
|
Cnm
|
Myopathy, Myotubular
|
Congenital Structural Myopathy
|
|
|
Rhabdomyosarcoma |
|
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 |
Lgmd2b
|
Muscular Dystrophy, Limb-Girdle, Type 2b
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e
|
Beta-Sarcoglycanopathy
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2y
|
Muscular Dystrophy, Limb-Girdle, Type 3
|
Lgmd3
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2s
|
LGMDR2
|
Muscular Dystrophy, Limb-Girdle, Type 2s
|
Limb-Girdle Muscular Dystrophy Type 2b
|
Lgmd2e
|
Limb-Girdle Muscular Dystrophy Due To Beta-Sarcoglycan Deficiency
|
Muscular Dystrophy, Limb-Girdle, Type 2e
|
Lgmd2s
|
Autosomal Recessive Muscular Dystrophy Due To Lap1b Deficiency
|
Autosomal Recessive Muscular Dystrophy Due To Torsin-1a-Interacting Protein 1 Deficiency
|
Lgmd2y
|
Muscular Dystrophy With Progressive Weakness, Distal Contractures And Rigid Spine
|
Muscular Dystrophy, Limb-Girdle, Type 2y
|
Dysferlin-Related Limb-Girdle Muscular Dystrophy R2
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b
|
Dysferlin-Related Lgmd R2
|
Lgmd Due To Dysferlin Deficiency
|
Lgmd Type 2b
|
Limb-Girdle Muscular Dystrophy Due To Dysferlin Deficiency
|
Limb-Girdle Muscular Dystrophy 2b
|
Limb-Girdle Muscular Dystrophy, Type 2b
|
Dystrophy, Muscular, Limb-Girdle, Autosomal Recessive, Type 2
|
Dystrophy, Muscular, Limb-Girdle, Type 2b
|
Limb-Girdle Muscular Dystrophy, Type 2e
|
|
|
Batten-Turner Congenital Myopathy |
Congenital Myopathy
|
Batten Turner Congenital Myopathy
|
Myopathy Congenital
|
Myopathy, Congenital
|
Myotonia Congenita
|
Benign Congenital Myopathy
|
|
|
Cutaneous Fibrous Histiocytoma |
Dermatofibroma
|
Fibrohistiocytic Tumor
|
Benign Cutaneous Fibrous Histiocytoma
|
Fibrous Histiocytoma Of Skin
|
Fibrous Xanthoma Of Skin
|
Pleomorphic Fibroma
|
Sclerosing Angioma
|
Sclerosing Angioma Of Skin
|
Fibrous Histiocytoma
|
|
|
Chordoma |
CHDM
|
Notochordoma
|
Notochordal Sarcoma
|
Chordoma, Susceptibility To
|
Chordocarcinoma
|
Chordoepithelioma
|
|
|
Rhabdoid Cancer |
Rhabdoid Tumor
|
Malignant Rhabdoid Tumor
|
Malignant Rhabdoid Tumour
|
Rhabdoid Sarcoma
|
Rhabdoid Tumor Predisposition Syndrome 1
|
Rhabdoid Tumor Predisposition Syndrome 2
|
Atypical Teratoid Rhabdoid Tumor
|
Brain Tumor, Posterior Fossa, Of Infancy, Familial
|
Atypical Teratoid/Rhabdoid Tumor
|
|
|
Muscular Dystrophy-Dystroglycanopathy , Type C, 7 |
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2u
|
Lgmd2u
|
MDDGC7
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 20
|
Lgmdr20
|
Muscular Dystrophy, Limb-Girdle, Type 2u
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Due To Ispd Deficiency
|
Muscular Dystrophy Limb-Girdle Type 2u
|
Muscular Dystrophy-Dystroglycanopathy Type C7
|
Ispd-Related Limb-Girdle Muscular Dystrophy R20
|
Ispd-Related Lgmd R20
|
Lgmd Type 2u
|
Limb-Girdle Muscular Dystrophy Type 2u
|
Muscular Dystrophy-Dystroglycanopathy Limb-Girdle C7
|
Dystrophy, Muscular, Dystroglycanopathy, Type C7
|
|
|
Muscular Dystrophy-Dystroglycanopathy , Type C, 14 |
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2t
|
Lgmd2t
|
MDDGC14
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 19
|
Lgmdr19
|
Muscular Dystrophy Limb-Girdle Type 2t
|
Muscular Dystrophy-Dystroglycanopathy Limb-Girdle Gmppb-Related
|
Muscular Dystrophy, Limb-Girdle, Type 2t
|
Muscular Dystrophy-Dystroglycanopathy, Limb-Girdle, Gmppb-Related
|
Muscular Dystrophy-Dystroglycanopathy Type C14
|
Gmppb-Related Limb-Girdle Muscular Dystrophy R19
|
Gmppb-Related Lgmd R19
|
Lgmd Type 2t
|
Limb-Girdle Muscular Dystrophy Type 2t
|
Muscular Dystrophy-Dystroglycanopathy Limb-Girdle C14
|
Dystrophy, Muscular, Limb-Girdle, Type 2t
|
|
|
Rhabdomyosarcoma 2 |
Alveolar Rhabdomyosarcoma
|
Rhabdomyosarcoma, Alveolar
|
Rhabdomyosarcoma Alveolar
|
RMS2
|
Rmsa
|
Rhabdomyosarcoma 2, Alveolar
|
Alveolar Childhood Rhabdomyosarcoma
|
Arms
|
Rhabdomyosarcoma, Type 2
|
|
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2w |
Lgmd2w
|
Muscular Dystrophy, Limb-Girdle, Type 2w
|
|
|
Fibrosarcoma |
Neoplasms, Fibrous Tissue
|
Fibrocytic Tumor
|
Fibrosarcoma Of Soft Tissue
|
Fibrous Tissue Neoplasm
|
|
|
Pulmonary Blastoma |
Blastoma Of Lung
|
Pneumoblastoma
|
|
|
Syringoma |
|
|
Muscular Dystrophy-Dystroglycanopathy , Type C, 9 |
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2p
|
Lgmd2p
|
MDDGC9
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 16
|
Lgmdr16
|
Muscular Dystrophy-Dystroglycanopathy Limb-Girdle Dag1-Related
|
Muscular Dystrophy, Limb-Girdle, Type 2p
|
Muscular Dystrophy-Dystroglycanopathy, Limb-Girdle, Dag1-Related
|
Muscular Dystrophy-Dystroglycanopathy Type C9
|
Alpha-Dystroglycan-Related Limb-Girdle Muscular Dystrophy R16
|
Alpha-Dystroglycan-Related Lgmd R16
|
Lgmd Type 2p
|
Limb-Girdle Muscular Dystrophy Type 2p
|
Muscular Dystrophy-Dystroglycanopathy Limb-Girdle C9
|
Muscular Dystrophy Limb-Girdle Type 2p
|
Dystrophy, Muscular, Limb-Girdle, Type 2p
|
|
|
Central Core Disease Of Muscle |
Central Core Disease
|
Central Core Myopathy
|
CCD
|
Cco
|
Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber
|
Myopathy, Central Core
|
Shy-Magee Syndrome
|
Muscle Core Disease
|
Muscular Central Core Disease
|
Myopathy, Central Fibrillar
|
Shy'S Disease
|
Moderate Multiminicore Disease With Hand Involvement
|
|
|
Nephroma |
|
|
Adenomatoid Tumor |
Adenomatoid Tumour
|
Benign Localised Epithelial Mesothelioma
|
Benign Localized Epithelial Mesothelioma
|
|
|
Neuroleptic Malignant Syndrome |
|
|
Muscular Dystrophy |
Muscular Dystrophies
|
Congenital Md
|
Congenital Muscular Dystrophy
|
Cmd
|
Mdc
|
Dystrophy, Muscular
|
Gower'S Muscular Dystrophy
|
Progressive Musclular Dystrophy
|
Pseudohypertrophic Atrophy
|
Pseudohypertrophic Muscle Paralysis
|
Pseudohypertrophic Muscular Atrophy
|
Pseudohypertrophic Muscular Dystrophy
|
Pseudohypertrophic Paralysis
|
Pseudomuscular Hypertrophy
|
|
|
Sertoli-Leydig Cell Tumor |
Sertoli-Leydig Cell Tumors
|
Androblastoma Of Ovary
|
Arrhenoblastoma
|
Arrhenoblastoma Of Ovary
|
Sertoli-Leydig Cell Tumor Of The Ovary
|
Sertoli-Leydig Cell Tumor Of Intermediate Differentiation
|
Sertoli-Leydig Cell Tumor Of Ovary
|
|
|
Perineurioma |
|
|
Myoepithelioma |
Benign Myoepithelioma
|
Myoepithelial Adenoma
|
Myoepithelial Neoplasm
|
Malignant Myoepithelioma
|
|
|
Limb-Girdle Muscular Dystrophy |
Lgmd
|
Limb Girdle Muscular Dystrophy
|
Muscular Dystrophies, Limb-Girdle
|
Erb'S Muscular Dystrophy
|
Leyden-Mbius Muscular Dystrophy
|
Limb-Girdle Syndrome
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Myopathic Limb-Girdle Syndrome
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Limb Girdle
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Muscular Dystrophy Limb-Girdle
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Dystrophy, Muscular, Limb-Girdle
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Lgmd - [Limb-Girdle Muscular Dystrophy]
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Limb Girdle Muscle Dystrophy
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Limb-Girdle Myopathy
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Immunodeficiency 48 |
Combined Immunodeficiency Due To Zap70 Deficiency
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IMD48
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Selective T-Cell Defect
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Stcd
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Zeta-Associated-Protein 70 Deficiency
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Severe Combined Immunodeficiency, Atypical
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Immunodeficiency, Type 48
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Zap70 Deficiency
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Leiomyomatosis |
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Echinostomiasis |
Infection By Echinochasmus
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Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1 |
Muscular Dystrophy, Limb-Girdle, Type 1e
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Lgmd1d
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Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1d
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LGMDD1
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Lgmd1e
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Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1
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Limb-Girdle Muscular Dystrophy Type 1d
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Muscular Dystrophy, Limb-Girdle, Type 1d
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Muscular Dystrophy, Limb-Girdle, Type 1d, Formerly
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Lgmd1d, Formerly
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Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1e
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Muscular Dystrophy Limb-Girdle Type 1d
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Muscular Dystrophy Limb-Girdle Type 1e
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Dnajb6-Related Limb-Girdle Muscular Dystrophy D1
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Dnajb6-Related Lgmd D1
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Lgmd Type 1d
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Limb-Girdle Muscular Dystrophy 1e
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Limb-Girdle Muscular Dystrophy-1d, Autosomal Dominant
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Dystrophy, Muscular, Limb-Girdle, Autosomal Dominant, Type 1
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Dystrophy, Muscular, Limb-Girdle, Type 1e
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Benign Giant Cell Tumor |
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Lipomatosis, Multiple |
Lipoma
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Familial Multiple Lipomatosis
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Lipomatosis, Familial Multiple
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Benign Lipomatous Tumor
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Lipomatous Neoplasm
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Multiple Lipomatosis
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Fml
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Lipo
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Benign Tumor Of Adipose Tissue
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Lipomatous Tumor
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Tumor Of Adipose Tissue
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Neoplasms, Adipose Tissue
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Lipomas
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Desmoid Tumor |
Aggressive Fibromatosis
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Desmoid Type Fibromatosis
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Familial Infiltrative Fibromatosis
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Desmoid Disorder, Hereditary
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Fif
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Fibromatosis, Familial Infiltrative
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Deep Fibromatosis
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Desmoid Fibromatosis
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Hereditary Desmoid Disease
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Musculoaponeurotic Fibromatosis
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Desmoid-Type Fibromatosis
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Fibromatosis, Aggressive
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Desmoid Disease, Hereditary
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Musculo-Aponeurotic Fibromatosis
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Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3 |
Lgmd1g
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Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1g
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LGMDD3
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Muscular Dystrophy, Limb-Girdle, Type 1g
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Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 3
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Limb-Girdle Muscular Dystrophy, Type 1g
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Muscular Dystrophy Limb-Girdle Type 1g
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Hnrnpdl-Related Limb-Girdle Muscular Dystrophy D3
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Hnrnpdl-Related Lgmd D3
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Lgmd Type 1g
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Limb-Girdle Muscular Dystrophy Type 1g
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Limb-Girdle Muscular Dystrophy 1g
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Dystrophy, Muscular, Limb-Girdle, Type 1g
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Neurilemmoma |
Schwannoma
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Benign Schwannoma
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Neurilemoma
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Peripheral Fibroblastoma
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Psammomatous Schwannoma
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Neurolemmoma
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Schwannomas
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Castleman Disease |
Angiofollicular Ganglionic Hyperplasia
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Angiofollicular Lymph Hyperplasia
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Giant Lymph Node Hyperplasia
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Castleman'S Disease
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Angiofollicular Lymph Node Hyperplasia
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Lymphoid Hamartoma
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Benign Giant Lymphoma
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Angiolymphoid Hyperplasia
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Fasciitis |
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Atrial Standstill 1 |
ATRST1
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Atrial Cardiomyopathy With Heart Block
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Cardiomyopathy, Familial, With Conduction Disturbance
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Atrial Standstill, Digenic
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Familial Cardiomyopathy With Conduction Disturbance
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Standstill, Atrial, Type 1
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Heart Block
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Cardiomyopathies
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Idiopathic Cardiomyopathy
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Idiopathic Cardiopathy
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Primary Myocardial Disease
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Primary Cardiomyopathy
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Myocardiopathy
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Myocardosis
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Primary Idiopathic Myocardial Disease
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Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g |
Lgmd2g
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Limb-Girdle Muscular Dystrophy Due To Telethonin Deficiency
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Muscular Dystrophy, Limb-Girdle, Type 2g
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Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j |
Lgmd2j
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Muscular Dystrophy, Limb-Girdle, Type 2j
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Coffin-Siris Syndrome 1 |
Coffin-Siris Syndrome
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Fifth Digit Syndrome
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Css
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CSS1
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Mrd12
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Mental Retardation, Autosomal Dominant 12
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Hhid
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Dwarfism-Onychodysplasia
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Hypertrichosis, Hyperkeratosis, Mental Retardation, And Distinctive Facial Features
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Autosomal Dominant Mental Retardation 12
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Short Stature-Onychodysplasia.
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Intellectual Disability With Absent Fifth Fingernail And Terminal Phalanx
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Mental Retardation With Hypoplastic Fifth Fingernails And Toenails
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Short Stature-Onychodysplasia
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Coffin-Siris Syndrome, Type 1
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Mental Retardation, Autosomal Dominant, Type 12
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Sarcoma, Synovial |
Synovial Sarcoma
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Synovialosarcoma
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Synovial Cell Sarcoma
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Sarcoma Synovial
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Pneumothorax |
Pneumothorax Nos
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Air Leak Nos
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Pleural Air Leak Nos
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Myasthenic Syndrome, Congenital, 6, Presynaptic |
Familial Infantile Myasthenia
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CMS6
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Cmsea
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Congenital Myasthenic Syndrome 6
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Familial Infantile Myasthenia Gravis 2
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Fimg2
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Myasthenic Syndrome, Congenital, Associated With Episodic Apnea
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Myasthenic Syndrome, Presynaptic, Congenital, Associated With Episodic Apnea
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Congenital Myasthenic Syndrome Type Ia2, Formerly
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Cms1a2, Formerly
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Cms Ia2, Formerly
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Myasthenia, Familial Infantile, Formerly
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Fim, Formerly
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Myasthenia Gravis, Familial Infantile, 2, Formerly
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Fimg2, Formerly
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Cms Ia2
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Cms1a2
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Congenital Myasthenic Syndrome 6, Presynaptic
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Congenital Myasthenic Syndrome Type Ia2
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Congenital Presynaptic Myasthenic Syndrome Associated With Episodic Apnea
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Fim
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Cms1a
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Cms-Ea
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Cms Ia
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Congenital Myasthenic Syndrome Pre-Synaptic Associated With Episodic Apnea
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Congenital Myasthenic Syndrome Type 1a
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Congenital Myasthenic Syndrome Type Ia
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Myasthenic Syndrome, Congenital, Type 6, Presynaptic
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Lipodystrophy, Familial Partial, Type 6 |
FPLD6
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Lipe-Related Familial Partial Lipodystrophy
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Familial Partial Lipodystrophy Type 6
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Lipe-Related Fpld
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Lipodystrophy, Familial Partial, Associated With Lipe Mutations
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Familial Partial Lipodystrophy Associated With Lipe Mutations
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Lipodystrophy, Familial Partial, 6
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Myopathy, Myofibrillar, 3 |
Myotilinopathy
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Myofibrillar Myopathy 3
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MFM3
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Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1a
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Lgmd1a
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Muscular Dystrophy, Limb-Girdle, Type 1a
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Myopathy, Myofibrillar, Myotilin-Related
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Muscular Dystrophy, Limb-Girdle, Type 1, Formerly
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Lgmd1, Formerly
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Muscular Dystrophy, Limb-Girdle, Type 1a, Formerly
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Lgmd1a, Formerly
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Qualitative Or Quantitative Defects Of Myotilin
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Limb-Girdle Muscular Dystrophy Due To Myotilin Deficiency
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Distal Myotilinopathy
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Lgmd1
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Limb-Girdle Muscular Dystrophy 1a
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Mfm Myotilin-Related
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Muscular Dystrophy, Limb-Girdle, Type 1
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Myopathy Myofibrillar Myotylin-Related
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Myopathy, Myofibrillar, Type 3
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Medulloblastoma |
MDB
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Cpnet
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Localized Primitive Neuroectodermal Tumor
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Classic Medulloblastoma
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Medulloblastoma Predisposition Syndrome
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Medulloblastoma, Somatic
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Brain Medulloblastoma
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Cns Pnet
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Infratentorial Primitive Neuroectodermal Tumor
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Neuroectodermal Tumors, Primitive
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Medulloblastomas
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Desmoplastic Medulloblastoma
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Medulloblastoma, With Extensive Nodularity
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Medulloblastoma Of Unspecified Site
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Medullomyoblastoma Of Unspecified Site
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Achalasia |
Cardiospasm
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Achalasia Of Cardia
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Esophageal Achalasia
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Hypertensive Lower Esophageal Sphincter
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Idiopathic Achalasia
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Achalasia Cardia
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Idiopathic Achalasia Of Esophagus
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Primary Achalasia
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Achalasia Of Esophagus
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Lack Of Reflex Relaxation Of Lower Oesophageal Sphincter
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Aperistalsis Of The Oesophagus
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Achalasia Of Oesophagus
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Oesophageal Achalasia
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Achalasia Nos
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Cardia Spasm
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Cardia Achalasia
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Oesophageal Cardiospasm
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Oesophagus Achalasia
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Reflex Cardiospasm
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Hypertrophic Cardiomyopathy |
Hypertrophic Obstructive Cardiomyopathy
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Cardiomyopathy, Hypertrophic
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Cardiomyopathy Hypertrophic Obstructive
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Cardiomyopathy, Hypertrophic, Familial
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Idiopathic Myocardial Hypertrophy
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Idiopathic Hypertrophic Cardiomyopathy
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Obstructive Idiopathic Hypertrophic Cardiomyopathy
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Obstructive Cardiomyopathy
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Idiopathic Hypertrophic Subaortic Stenosis
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Muscular Subaortic Stenosis
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Hypertrophic Obstructive Subaortic Stenosis
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Ewing Sarcoma |
Neuroepithelioma
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Ewing'S Tumor
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Primitive Neuroectodermal Tumor
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Ewings Sarcoma
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Ewing'S Sarcoma
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Peripheral Neuroepithelioma
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ES
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Ewings Sarcoma-Primitive Neuroectodermal Tumor
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Localized Peripheral Primitive Neuroectodermal Tumor
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Peripheral Primitive Neuroectodermal Tumor
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Ewing Tumor
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Sarcoma, Ewing'S
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Ewing Family Of Tumors
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Extraosseous Ewing Tumor
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Askin Tumor
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Ewing'S Family Localized Tumor
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Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor
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Localized Ewing Sarcoma
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Localized Ewing'S Sarcoma
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Localized Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor
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Localized Ewing'S Tumor
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Pnet Of Thoracopulmonary Region
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Tumor Of The Ewing Family
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Skeletal Ewing Sarcoma
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Osseous Ewing Sarcoma
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Ppnet
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Peripheral Pnet
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Extraskeletal Ewing Sarcoma
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Eoe
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Extraosseous Ewing Sarcoma
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Extraskeletal Ewing Tumor
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Esft
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Ewing Sarcoma Family Of Tumors
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Pne
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Pnet
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Pnet Of The Chest Wall
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Sarcoma, Ewing
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Neuroectodermal Tumors, Primitive, Peripheral
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Neuroectodermal Tumor, Primitive
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Disorder Of Eye
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Askin'S Tumor
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Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor
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Neuroepithelioma, Peripheral
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Cardiomyopathy, Dilated, 1h |
Dilated Cardiomyopathy 1h
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Dilated Cardiomyopathy With Conduction Defect
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CMD1H
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Cardiomyopathy, Dilated, With Conduction Defect
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Muscular Dystrophy, Duchenne Type |
Duchenne Muscular Dystrophy
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DMD
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Muscular Dystrophy, Duchenne
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Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type
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Severe Dystrophinopathy, Duchenne Type
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Muscular Dystrophy Duchenne
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Dystrophy, Muscular, Duchenne Type
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Benign Duchenne Muscular Dystrophy
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Duchenne Motor Neuron Disease
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Duchenne Type Dystrophy
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Duchenne-Griesinger Disease
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Constipation |
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