| 疾病名称 |
别名 |
|
| Werner Syndrome |
|
Werner'S Syndrome
|
WRN
|
|
Adult Progeria
|
Ws
|
|
Adult Premature Ageing Syndrome
|
Adult Premature Aging Syndrome
|
|
Werners Syndrome
|
|
|
| Fallopian Tube Disease |
|
|
| Spastic Paraplegia 84, Autosomal Recessive |
|
SPG84
|
Hereditary Spastic Paraplegia 84
|
|
Spastic Paraplegia 84 Autosomal Recessive
|
Doid:0112347
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Fanconi Anemia, Complementation Group A |
|
Fanconi Anemia
|
Fanconi Pancytopenia
|
|
Fanconi Anemia Complementation Group A
|
FANCA
|
|
Fa
|
Fanconi Panmyelopathy
|
|
Fanconi'S Anemia
|
Fanconi Anaemia
|
|
Fanconi'S Anaemia
|
Fanconi Hypoplastic Anemia
|
|
Estren-Dameshek Variant Of Fanconi Anemia
|
Estren-Dameshek Variant Of Fanconi Pancytopenia
|
|
Fanconi Anemia Estren-Dameshek Variant
|
Fanconis Anemia
|
|
|
| Endometrial Cancer |
|
Endometrial Carcinoma
|
Endometrial Neoplasm
|
|
Malignant Neoplasm Of Endometrium
|
Endometrioid Carcinoma
|
|
Endometrial Neoplasms
|
Carcinoma, Endometrioid
|
|
Endometrial Cancer, Familial
|
Endometrial Carcinoma, Somatic
|
|
Endometrial Cancer, Susceptibility To
|
Endometrial Ca
|
|
Malignant Endometrial Neoplasm
|
Neoplasm Of Endometrium
|
|
Primary Malignant Neoplasm Of Endometrium
|
Tumor Of Endometrium
|
|
Carcinoma Of The Endometrium
|
Endometrioid Carcinoma Of Female Reproductive System
|
|
ENDMC
|
Carcinoma Endometrioid
|
|
Endometrial Cancers
|
Cancer, Endometrial
|
|
Uterine Corpus Cancer
|
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
|
Microcephalic
|
Nanocephaly
|
|
Congenital Microcephaly
|
Brain Hypoplasia
|
|
Brain Nondevelopment
|
Cephalic Hypoplasia
|
|
Undeveloped Cerebrum
|
Undeveloped Brain
|
|
Micrencephalon
|
Micrencephaly
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Pontocerebellar Hypoplasia, Type 2e |
|
Pontocerebellar Hypoplasia Type 2
|
Pontocerebellar Hypoplasia Type 2e
|
|
Pch2
|
PCH2E
|
|
Progressive Microcephaly From Birth Extrapyramidal Dyskinesia Chorea Epilepsy
|
Pontocerebellar Hypoplasia 2e
|
|
Pcca2
|
Progressive Cerebello-Cerebral Atrophy Type 2
|
|
Doid:0112328
|
Hypoplasia, Pontocerebellar, Type 2e
|
|
Pontocerebellar Hypoplasia, Type 2d
|
Pontocerebellar Hypoplasia Type 2a
|
|
|
| Immunodeficiency 25 |
|
Immunodeficiency Due To Defect In Cd3-Zeta
|
IMD25
|
|
Immunodeficiency, Type 25
|
|
|
| Autosomal Recessive Cerebellar Ataxia |
|
|
| Alternating Hemiplegia Of Childhood |
|
Alternating Hemiplegia
|
Ahc
|
|
Alternating Hemiplegia Syndrome
|
Hemiplegia, Alternating, Of Childhood
|
|
Hemiplegia, Crossed
|
|
|
| Spastic Paraplegia 85, Autosomal Recessive |
|
SPG85
|
Hereditary Spastic Paraplegia 85
|
|
Spastic Paraplegia 85 Autosomal Recessive
|
Doid:0112345
|
|
|
| Sporadic Breast Cancer |
|
Sporadic Breast Carcinoma
|
|
|
| Pontocerebellar Hypoplasia |
|
Pch
|
Congenital Pontocerebellar Hypoplasia
|
|
Opch
|
Hypoplasia, Pontocerebellar
|
|
Pontoneocerebellar Hypoplasia
|
Nonsyndromic Pontocerebellar Hypoplasia
|
|
|
| Spastic Paraplegia 86, Autosomal Recessive |
|
SPG86
|
Hereditary Spastic Paraplegia 86
|
|
Spastic Paraplegia 86 Autosomal Recessive
|
Doid:0112342
|
|
|
| Li-Fraumeni Syndrome |
|
Sarcoma Family Syndrome Of Li And Fraumeni
|
Sbla Syndrome
|
|
LFS
|
Li-Fraumeni Familiar Cancer Susceptibility Syndrome
|
|
Sarcoma, Breast, Leukaemia And Adrenal Gland Syndrome
|
Lfs1
|
|
Li Fraumeni Syndrome
|
Sarcoma, Breast, Leukemia, And Adrenal Gland Syndrome
|
|
Lfl
|
Sbla Syndrome Li-Fraumeni-Like Syndrome
|
|
Li-Fraumeni Syndrome 1
|
|
|
| Fanconi Anemia, Complementation Group R |
|
Fanconi Anemia Complementation Group R
|
FANCR
|
|
|
| Hereditary Breast Ovarian Cancer Syndrome |
|
Hereditary Breast And Ovarian Cancer Syndrome
|
Brca1- And Brca2-Associated Hereditary Breast And Ovarian Cancer
|
|
Breast And/Or Ovarian Cancer
|
Breast And Ovarian Cancer Syndrome
|
|
Hboc Syndrome
|
Hereditary Breast And Ovarian Cancer
|
|
Brca1- Brca2-Associated Hboc
|
|
|
| Neuroma |
|
|
| Bloom Syndrome |
|
BLM
|
Bs
|
|
Bls
|
Bloom-Torre-Machacek Syndrome
|
|
Microcephaly, Growth Restriction, And Increased Sister Chromatid Exchange 1
|
Mgrisce1
|
|
Congenital Telangiectatic Erythema
|
Congenital Telangiectatic Erythema Syndrome
|
|
Growth Deficiency, Sun-Sensitive, Telangiectatic, Hypo And Hyperpigmented Skin, Predisposition To Malignancy And Chromosomal Instability
|
Bloom'S Syndrome
|
|
Bsyn
|
|
|
| Fanconi Anemia, Complementation Group D2 |
|
Fanconi Anemia Complementation Group D2
|
FANCD2
|
|
Fad2
|
Fa4
|
|
Fancd
|
Fanconi Pancytopenia Type 4
|
|
Fanconi Anemia, Complementation Group D
|
Fanconi Pancytopenia, Type 4
|
|
Facd
|
Fanconi Anemia Complementation Group D
|
|
|
| Haverhill Fever |
|
Streptobacillosis
|
Streptobacillary Rat-Bite Fever
|
|
Streptobacillary Fever
|
Rat-Bite Fever Due To Streptobacillus Moniliformis
|
|
Erythema Arthriticum Epidemicum
|
Epidemic Arthritic Erythema
|
|
|
| Physical Disorder |
|
|
| Aplastic Anemia |
|
Aplastic Anemia, Susceptibility To
|
Anemia Aplastic
|
|
Idiopathic Aplastic Anemia
|
Secondary Aplastic Anemia
|
|
Idiopathic Bone Marrow Failure
|
Aplastic Anemia Idiopathic
|
|
AA
|
Anemia, Aplastic
|
|
Aplastic Anemia, Idiopathic
|
Erythroid Aplasia
|
|
Aa - [Aplastic Anaemia]
|
Haematopoietic Aplasia
|
|
Aleukia Haemorrhagica
|
Anaemia Due To Decreased Red Cell Production
|
|
Aplasia Bone Marrow
|
Aplastic Bone Marrow
|
|
Hypoplastic Anaemia Nos
|
Myeloid Bone Marrow Aplasia
|
|
Pancytopenia
|
Panhaematopenia
|
|
Hypoproliferative Anaemia
|
Medullary Hypoplasia
|
|
Red Blood Cells Hypoplastic Anaemia
|
Panmyelophthisis
|
|
Panhemocytopenia
|
Refractive Hypoproliferative Anaemia
|
|
Toxic Anaemia
|
Toxic Aplastic Anaemia
|
|
Aplastic Anaemia Due To Toxic Cause
|
Idiopathic Aplastic Anaemia Nos
|
|
|
| Rothmund-Thomson Syndrome, Type 2 |
|
Rothmund-Thomson Syndrome
|
Rts
|
|
RTS2
|
Poikiloderma Of Rothmund-Thomson
|
|
Rothmund-Thomson Syndrome Type 2
|
Congenital Poikiloderma
|
|
Poikiloderma Congenitale
|
Poikiloderma Atrophicans And Cataract
|
|
Poikiloderma Congenitale Of Rothmund-Thomson
|
Poikiloderma Of Rothmund-Thomson Type 2
|
|
Rothmund-Thomson Syndrome 2
|
Erythrokeratodermia Variabilis
|
|
|
| Trichohepatoenteric Syndrome 1 |
|
Trichohepatoenteric Syndrome
|
Syndromic Diarrhea
|
|
Tricho-Hepato-Enteric Syndrome
|
Sd/The
|
|
Syndromic Diarrhea/Tricho-Hepato-Enteric Syndrome
|
THES1
|
|
Phenotypic Diarrhea
|
Thes
|
|
Phenotypic Diarrhea Of Infancy
|
Diarrhea, Syndromic
|
|
Diarrhea, Fatal Infantile, With Trichorrhexis Nodosa
|
Intractable Diarrhea With Phenotypic Anomalies
|
|
Syndromatic Diarrhea
|
Fatal Infantile Diarrhea With Trichorrhexis Nodosa
|
|
|
| Xeroderma Pigmentosum, Variant Type |
|
Xeroderma Pigmentosum
|
XPV
|
|
Xeroderma Pigmentosum Variant Type
|
Xeroderma Pigmentosum With Normal Dna Repair Rates
|
|
Photosensitivity With Defective Dna Synthesis
|
De Sanctis-Cacchione Syndrome
|
|
Xp
|
Desanctis-Cacchione Syndrome
|
|
Xeroderma Pigmentosa
|
Xerodermic Idiocy
|
|
Xeroderma Pigmentosum Variant
|
Xp - [Xeroderma Pigmentosum]
|
|
Atrophoderma Pigmentosum
|
|
|
| Leukemia, Acute Myeloid |
|
Acute Myeloid Leukemia
|
Leukemia, Acute Myelogenous
|
|
Acute Myelogenous Leukemia
|
AML
|
|
Leukemia, Acute Myeloid, Susceptibility To
|
Acute Myeloblastic Leukemia
|
|
Leukemia, Acute Myeloid, Reduced Survival In, Somatic
|
Acute Myeloid Leukaemia
|
|
Leukemia, Myelocytic, Acute
|
Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome
|
|
Secondary Aml
|
Acute Myelocytic Leukemia
|
|
Leukemia, Myeloid, Acute
|
Acute Myeloid Leukemia, Somatic
|
|
Leukemia, Acute Myeloid, Somatic
|
Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic
|
|
Acute Myeloblastic Leukaemia
|
Acute Myelogenous Leukaemia
|
|
Aml - Acute Myeloid Leukemia
|
Acute Myeloid Leukemia With Cebpa Somatic Mutations
|
|
Aml With Cebpa Somatic Mutations
|
Inherited Acute Myeloid Leukemia
|
|
Familial Aml
|
Inherited Aml
|
|
Pure Familial Aml
|
Pure Familial Acute Myeloid Leukemia
|
|
Secondary Acute Myeloid Leukemia
|
Therapy-Related Aml And Myelodysplastic Syndrome
|
|
Acute Myeloid Leukemia, Secondary
|
Acute Non-Lymphoblastic Leukemia
|
|
Acute Non-Lymphocytic Leukemia
|
Acute Biphenotypic Leukemia
|
|
Acute Undifferentiated Leukemia
|
Acute Myeloblastic Leukaemia With Multilineage Dysplasia
|
|
Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission
|
Acute Myeloid Leukaemia With Myelodysplasia-Related Features
|
|
|
| Glanders |
|
Farcy Pipes
|
Infection Due To Pseudomonas Mallei
|
|
Burkholderia Mallei
|
Burkholderia Mallei Infection
|
|
Equina
|
Equine Glanders
|
|
Farcy
|
Farcy Buds
|
|
Farcy Cords
|
Infection Due To Actinobacillus Mallei
|
|
Infection Due To Malleomyces Mallei
|
Maliasmus
|
|
Malleus
|
Farce
|
|
Actinobacillosis
|
Actinobacillus Infection
|
|
|
| Ataxia-Telangiectasia |
|
Ataxia Telangiectasia
|
Louis-Bar Syndrome
|
|
AT
|
At1
|
|
Ataxia-Telangiectasia Syndrome
|
Ataxia - Telangiectasia Variant
|
|
Boder-Sedgwick Syndrome
|
Louis Bar Syndrome
|
|
Cerebello-Oculocutaneous Telangiectasia
|
Immunodeficiency With Ataxia Telangiectasia
|
|
A-T
|
Ataxia Telangiectasia Syndrome
|
|
Atm
|
Telangiectasia, Cerebello-Oculocutaneous
|
|
Ataxia-Telangiectasia Variant
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Breast Cancer, Familial
|
|
Malignant Neoplasm Of Breast
|
Male Breast Cancer
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Lynch Syndrome |
|
Hereditary Nonpolyposis Colon Cancer
|
Hereditary Nonpolyposis Colorectal Cancer
|
|
Hereditary Nonpolyposis Colorectal Carcinoma
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
|
Familial Nonpolyposis Colon Cancer
|
Hnpcc
|
|
Coca 1
|
Hereditary Defective Mismatch Repair Syndrome
|
|
Hereditary Non-Polyposis Colon Cancer
|
Hereditary Non-Polyposis Colon Cancer Syndrome
|
|
Hereditary Non-Polyposis Colorectal Cancer
|
Hereditary Non-Polyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colon Cancer Syndrome
|
Hereditary Nonpolyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colorectal Neoplasm
|
Hnpcc - Hereditary Nonpolyposis Colon Cancer
|
|
Cancer Family Syndrome
|
Familial Nonpolyposis Colorectal Cancer
|
|
Colon Cancer, Familial Nonpolyposis
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
|
Cancer, Colorectal, Nonpolyposis, Hereditary
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
|
|
| Fanconi Anemia, Complementation Group D1 |
|
Fanconi Anemia Complementation Group D1
|
FANCD1
|
|
Fad1
|
Inherited Cancer-Predisposing Syndrome Due To Biallelic Brca2 Mutations
|
|
|
| Cerebellar Disease |
|
Cerebellar Diseases
|
Cerebellar Dysfunction
|
|
Cerebellar Abnormality
|
Cerebellar Disorders
|
|
|
| Mirror Movements 1 |
|
Congenital Mirror Movement Disorder
|
Bimanual Synergia
|
|
Congenital Mirror Movements
|
Familial Congenital Controlateral Synkinesia
|
|
Familial Congenital Mirror Movements
|
Hereditary Congenital Controlateral Synkinesia
|
|
Hereditary Congenital Mirror Movements
|
Isolated Congenital Controlateral Synkinesia
|
|
Isolated Congenital Mirror Movements
|
Mirror Movements
|
|
MRMV1
|
Mirror Movements 1 And/Or Agenesis Of The Corpus Callosum
|
|
Mirror Movements, Congenital
|
Bimanual Synkinesis
|
|
Cmm
|
Mirror Movements, Type 1
|
|
|
| Trichothiodystrophy |
|
Ttd
|
Amish Brittle Hair Syndrome
|
|
Bids Syndrome
|
Brittle Hair-Intellectual Impairment-Decreased Fertility-Short Stature Syndrome
|
|
Ibids
|
Pibids
|
|
Trichothiodystrophy Syndromes
|
|
|
| Nijmegen Breakage Syndrome |
|
Berlin Breakage Syndrome
|
NBS
|
|
Microcephaly, Normal Intelligence And Immunodeficiency
|
Ataxia-Telangiectasia Variant
|
|
Ataxia-Telangiectasia Variant V1
|
Seemanova Syndrome Ii
|
|
Immunodeficiency-Microcephaly-Chromosomal Instability Syndrome
|
Seemanova Syndrome Type 2
|
|
At-V1
|
Microcephaly With Normal Intelligence, Immunodeficiency, And Lymphoreticular Malignancies
|
|
Nonsyndromal Microcephaly, Autosomal Recessive, With Normal Intelligence
|
Immunodeficiency, Microcephaly, And Chromosomal Instability
|
|
Microcephaly-Immunodeficiency-Lymphoreticuloma Syndrome
|
Microcephaly Immunodeficiency Lymphoreticuloma
|
|
Microcephaly With Normal Intelligence Immunodeficiency And Lymphoreticular Malignancies
|
Nonsyndromal Microcephaly Autosomal Recessive With Normal Intelligence
|
|
Seemanova Syndrome 2
|
Ataxia-Telangiectasia Variant 1
|
|
Seemanova Syndrome
|
At V1
|
|
Ataxia-Telangiectasia, Variant 1
|
Microcephaly-Immunodeficiency-Lymphoid Malignancy Syndrome
|
|
V-At
|
Ataxia Telangiectasia Variant V1
|
|
|
| Seckel Syndrome |
|
Microcephalic Primordial Dwarfism
|
Bird-Headed Dwarfism
|
|
Harper'S Syndrome
|
Virchow-Seckel Dwarfism
|
|
Nanocephalic Dwarfism
|
Sckl
|
|
Seckel-Type Dwarfism
|
|
|
| Parkinsonism With Spasticity, X-Linked |
|
X-Linked Parkinsonism-Spasticity Syndrome
|
XPDS
|
|
X-Linked Parkinsonism With Spasticity
|
|
|
| Cockayne Syndrome A |
|
Cockayne Syndrome Type 1
|
Cockayne Syndrome, Type A
|
|
Cockayne Syndrome Type I
|
CSA
|
|
Cockayne Syndrome Classic Form
|
Cockayne Syndrome Classical
|
|
Cockayne Syndrome Type A
|
Ckn1
|
|
|
| Bilateral Breast Cancer |
|
Bilateral Breast Carcinoma
|
|
|
| Medulloblastoma |
|
MDB
|
Cpnet
|
|
Localized Primitive Neuroectodermal Tumor
|
Classic Medulloblastoma
|
|
Desmoplastic/Nodular Medulloblastoma
|
Medulloblastoma With Extensive Nodularity
|
|
Desmoplastic Medulloblastoma
|
Medulloblastoma, Somatic
|
|
Medulloblastoma, Desmoplastic
|
Brain Medulloblastoma
|
|
Cns Pnet
|
Infratentorial Primitive Neuroectodermal Tumor
|
|
Mben
|
Medulloblastoma Desmoplastic
|
|
Neuroectodermal Tumors, Primitive
|
Medulloblastomas
|
|
Medulloblastoma, With Extensive Nodularity
|
Medulloblastoma Of Unspecified Site
|
|
Medullomyoblastoma Of Unspecified Site
|
|
|
| Pancreatic Adenocarcinoma |
|
Adenocarcinoma Of Pancreas
|
Adenocarcinoma Of The Pancreas
|
|
Pancreas Adenocarcinoma
|
Malignant Exocrine Neoplasm
|
|
Primary Pancreatic Adenocarcinoma
|
Adenocarcinoma Of Islet Cell Of Pancreas
|
|
Islet Cell Adenocarcinoma Of Unspecified Site
|
Mixed Adenocarcinoma Islet Cell With Exocrine Of Unspecified Site
|
|
|
| Cervix Melanoma |
|
|
| Prostate Cancer |
|
Prostate Carcinoma
|
Prostate Cancer, Familial
|
|
Prostate Neoplasm
|
Prostate Cancer, Somatic
|
|
Prostate Cancer, Susceptibility To
|
Prostatic Cancer
|
|
Prostatic Neoplasms
|
Hereditary Prostate Cancer
|
|
Prostatic Neoplasm
|
Cancer Of Prostate
|
|
Carcinoma Of Prostate
|
Familial Prostate Cancer
|
|
Familial Prostate Carcinoma
|
Malignant Tumor Of Prostate
|
|
Malignant Neoplasm Of Prostate
|
Prostate Cancer, Familial, Susceptibility To
|
|
Malignant Tumor Of The Prostate
|
Ngp - New Growth Of Prostate
|
|
Tumor Of The Prostate
|
Prostate Cancer, Hereditary
|
|
Cancer Of The Prostate
|
Malignant Neoplasm Of The Prostate
|
|
Prostatic Carcinoma
|
PC
|
|
Prca
|
Cancer, Prostate
|
|
Malignant Prostatic Tumour
|
Malignant Tumour Of Prostate
|
|
Primary Prostate Cancer
|
Primary Malignant Neoplasm Of Prostate
|
|
Prostate Gland Cancer
|
|
|
| Ovarian Cancer |
|
Ovarian Carcinoma
|
Ovarian Neoplasm
|
|
Malignant Tumour Of Ovary
|
Epithelial Ovarian Cancer
|
|
Neoplasm Of Ovary
|
Ovarian Neoplasms
|
|
Ovarian Cancers
|
Malignant Neoplasm Of Ovary
|
|
Primary Malignant Neoplasm Of Ovary
|
Ovarian Cancer, Somatic
|
|
Malignant Ovarian Tumor
|
Ovary Neoplasm
|
|
Primary Ovarian Cancer
|
Tumor Of The Ovary
|
|
Cancer Of The Ovary
|
Malignant Neoplasm Of The Ovary
|
|
Malignant Tumor Of The Ovary
|
Ovarian Malignant Tumor
|
|
OC
|
Ovarian Carcinomas
|
|
Cancer, Ovarian
|
Cancer Of Ovary
|
|
Ovary Cancer
|
Ca Ovary
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| Mirror Movements 2 |
|
MRMV2
|
Mirror Movements, Type 2
|
|
|
| Cowden Syndrome |
|
Cowden Disease
|
Multiple Hamartoma Syndrome
|
|
Cowden'S Disease
|
Lhermitte-Duclos Disease
|
|
Cd
|
Cs
|
|
Mham
|
Dysplastic Gangliocytoma Of Cerebellum
|
|
Cowden'S Syndrome
|
Hamartoma Syndrome, Multiple
|
|
|
| Malignant Renovascular Hypertension |
|
Secondary Malignant Renovascular Hypertension
|
|
|
