| 疾病名称 |
别名 |
|
| Legius Syndrome |
|
Neurofibromatosis Type 1-Like Syndrome
|
Nfls
|
|
LGSS
|
Neurofibromatosis 1-Like Syndrome
|
|
Neurofibromatosis Type 1 Like Syndrome
|
Nf1-Like Syndrome
|
|
Neurofibromatosis, Type 1-Like Syndrome
|
|
|
| Noonan Syndrome And Noonan-Related Syndrome |
|
|
| Neurofibromatosis |
|
Neurofibromatoses
|
Acoustic Neurofibromatosis
|
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Central Neurofibromatosis
|
Peripheral Neurofibromatosis
|
|
Recklinghausen'S Neurofibromatosis
|
Von Reklinghausen Disease
|
|
Neurofibromatosis Type 1
|
|
|
| Hyperpigmentation With Or Without Hypopigmentation, Familial Progressive |
|
FPHH
|
Melanosis Universalis Hereditaria
|
|
Muh
|
Familial Progressive Hyperpigmentation With Or Without Hypopigmentation
|
|
Hyperpigmentation, Familial Progressive, 2, Formerly
|
Fph2, Formerly
|
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Hyperpigmentation With Or Without Hypopigmentation
|
Familial Progressive Hyper- And Hypopigmentation
|
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Hyperpigmentation, Familial Progressive
|
|
|
| Plexiform Neurofibroma |
|
Neurofibroma Plexiform
|
Neurofibroma, Plexiform
|
|
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| Pulsating Exophthalmos |
|
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| Neurofibromatosis-Noonan Syndrome |
|
NFNS
|
Neurofibromatosis Type 1
|
|
Neurofibromatosis With Noonan Phenotype
|
Nf1
|
|
Von Recklinghausen Disease
|
Neurofibromatosis Type 1-Noonan Syndrome
|
|
Noonan Neurofibromatosis Syndrome
|
Recklinghausen'S Disease
|
|
Noonan-Neurofibromatosis Syndrome
|
Fibromatosis Multiple Non Ossifying
|
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Disseminated Nonossifying Fibromas In Association With Cafe-Au-Lait Spots
|
Jaffe Campanacci Syndrome
|
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Type 1 Neurofibromatosis
|
Neurofibromatosis 1
|
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Peripheral Neurofibromatosis
|
Recklinghausen Disease, Nerve
|
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Jaffe-Campanacci Syndrome
|
|
|
| Noonan Syndrome With Multiple Lentigines |
|
Leopard Syndrome
|
Multiple Lentigines Syndrome
|
|
Moynahan Syndrome
|
Cardiomyopathic Lentiginosis
|
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Progressive Cardiomyopathic Lentiginosis
|
Cardio-Cutaneous Syndrome
|
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Lentiginosis Profusa
|
Capute-Rimoin-Konigsmark-Esterly-Richardson Syndrome
|
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Generalized Lentiginosis
|
Gorlin Syndrome Ii
|
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Lentiginosis Profusa Syndrome
|
Lentigines, Electrocardiographic Conduction Abnormalities, Ocular Hypertelorism, Pulmonic Stenosis, Abnormal Genitalia, Retardation Of Growth, Deafnes
|
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Diffuse Lentiginosis
|
Nsml
|
|
Familial Multiple Lentigines Syndrome
|
Alopecia-Epilepsy-Intellectual Disability Syndrome, Moynahan Type
|
|
Progressive Cardiomyopathic Lentiginosis Syndrome
|
Alopecia Epilepsy Oligophrenia Syndrome Of Moynahan
|
|
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| Skin Granular Cell Tumor |
|
Granular Cell Neoplasm Of The Skin
|
Granular Cell Tumor Of Skin
|
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Granular Cell Tumour Of Skin
|
Skin Granular Cell Tumour
|
|
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| Mucosal Melanoma |
|
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| Vulvar Melanoma |
|
Malignant Melanoma Of Vulva
|
|
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| Cardiofaciocutaneous Syndrome 1 |
|
Cardiofaciocutaneous Syndrome
|
Cfc Syndrome
|
|
Cardio-Facio-Cutaneous Syndrome
|
CFC1
|
|
Cfcs
|
Cardio-Facial-Cutaneous Syndrome
|
|
Congenital Heart Defects Characteristic Facial Appearance Ectodermal Abnormalities And Growth Failure
|
Cardiofaciocutaneous Syndrome, Type 1
|
|
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| Optic Nerve Glioma |
|
Glioma Of The Optic Nerve
|
|
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| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
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| Malignant Skin Fibrous Histiocytoma |
|
Vaginal Melanoma
|
Malignant Fibrous Histiocytoma Of Skin
|
|
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| Malignant Dermis Tumor |
|
Malignant Tumor Of Dermis
|
Malignant Dermis Tumour
|
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Malignant Neoplasm Of Dermis
|
Malignant Tumour Of Dermis
|
|
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| Attention Deficit-Hyperactivity Disorder |
|
Attention Deficit Hyperactivity Disorder
|
ADHD
|
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Attention Deficit Disorder
|
Attention Deficit-Hyperactivity Disorder, Susceptibility To
|
|
Attention Deficit Disorder With Hyperactivity
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Hyperkinetic Disorder
|
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Hyperactivity Of Childhood
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Attention-Deficit/Hyperactivity Disorder
|
|
Add
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Addh
|
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Attention Deficit
|
Attention Deficit Disorder Of Childhood With Hyperactivity
|
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Attention Deficit Disorder With Hyperactivity Syndrome
|
Hyperkinetic Syndrome
|
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Attention-Deficit Hyperactivity Disorder
|
Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
|
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Disturbance Of Activity And Attention
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Disorder Of Activity And Attention
|
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Adhd - [Attention Deficit Hyperactivity Disorder]
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Hyperkinetic Disorders
|
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Disorder Of Activity And Attention With Hyperkinesia
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Attention Deficit Syndrome With Hyperactivity
|
|
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| Optic Nerve Neoplasm |
|
Optic Nerve Neoplasms
|
Neoplasm Of Optic Nerve
|
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Tumor Of Second Cranial Nerve
|
Tumour Of Optic Nerve
|
|
|
| Neurilemmomatosis |
|
Schwannomatosis
|
Neurofibromatosis Type 3
|
|
Nf3
|
Neurilemmomatosis Congenital Cutaneous
|
|
Neurinomatosis
|
Congenital Cutaneous Neurilemmomatosis
|
|
Multiple Neurilemmomas
|
Multiple Schwannomas
|
|
Neurilemmomatosis, Congenital Cutaneous
|
Schwannomatosis 1
|
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Neurofibromatosis 3
|
Mixed Central And Peripheral Neurofibromatosis
|
|
Nf3 - [Neurofibromatosis Type 3]
|
|
|
| Costello Syndrome |
|
Faciocutaneoskeletal Syndrome
|
Fcs Syndrome
|
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Congenital Myopathy With Excess Of Muscle Spindles
|
CSTLO
|
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CMEMS
|
Fcss
|
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Myopathy, Congenital, With Excess Of Muscle Spindles
|
|
|
| Noonan Syndrome-Like Disorder With Loose Anagen Hair |
|
Noonan-Like Syndrome With Loose Anagen Hair
|
Mazzanti Syndrome
|
|
Ns/Lah
|
|
|
| Pulmonary Valve Stenosis |
|
Valvular Pulmonary Stenosis
|
Heart Valve Pulmonary Stenosis
|
|
Valvar Pulmonary Stenosis
|
Valvate Pulmonary Stenosis
|
|
Pulmonary Stenosis
|
Pulmonary Valve Stricture
|
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Pulmonic Valve Stenosis
|
Ps - [Pulmonary Valve Stenosis]
|
|
Pvs - [Pulmonary Valve Stenosis]
|
Pulmonary Valvular Stricture
|
|
Pulmonary Valvular Stenosis
|
Pulmonary Valvular Obstruction
|
|
Pulmonary Valve Obstruction
|
Obstructed Pulmonary Valve
|
|
|
| Pulmonary Valve Disease |
|
|
| Lipomatosis, Multiple |
|
Lipoma
|
Familial Multiple Lipomatosis
|
|
Lipomatosis, Familial Multiple
|
Benign Lipomatous Tumor
|
|
Lipomatous Neoplasm
|
Multiple Lipomatosis
|
|
Fml
|
Lipo
|
|
Benign Tumor Of Adipose Tissue
|
Lipomatous Tumor
|
|
Tumor Of Adipose Tissue
|
Neoplasms, Adipose Tissue
|
|
Lipomas
|
|
|
| Neurofibromatosis, Type I |
|
Von Recklinghausen Disease
|
Neurofibromatosis 1
|
|
Neurofibromatosis, Type 1
|
NF1
|
|
Neurofibromatosis, Peripheral Type
|
Neurofibromatosis Type I
|
|
Neurofibromatosis Type 1 Due To Nf1 Mutation Or Intragenic Deletion
|
Familial Spinal Neurofibromatosis
|
|
Fsnf
|
Peripheral Neurofibromatosis
|
|
Von Recklinghausen'S Neurofibromatosis
|
Von Recklinghausen Disease Due To Nf1 Mutation Or Intragenic Deletion
|
|
Neurofibromatosis Peripheral Type
|
Von Recklinghausen Syndrome
|
|
Neurofibromatosis Type 1
|
Von Recklinghausen Neuropathy
|
|
Nf1 - [Neurofibromatosis Type 1]
|
Recklinghausen Disease
|
|
|
| Learning Disability |
|
Learning Disabilities
|
Learning Disorders
|
|
Academic Skill Disorder
|
Learning Disorder
|
|
|
| Piebald Trait |
|
Piebaldism
|
PBT
|
|
Partial Albinism
|
Albinoidism, Oculocutaneous, Autosomal Dominant
|
|
|
| Gingival Fibromatosis |
|
Hereditary Gingival Fibromatosis
|
Hereditary Gingival Hyperplasia
|
|
Autosomal Dominant Gingival Fibromatosis
|
Autosomal Dominant Gingival Hyperplasia
|
|
Fibromatosis, Gingival, Hereditary
|
Fibromatosis, Gingival
|
|
|
| Juvenile Myelomonocytic Leukemia |
|
Leukemia, Juvenile Myelomonocytic
|
JMML
|
|
Leukemia, Juvenile Myelomonocytic, Somatic
|
Juvenile Chronic Myelomonocytic Leukemia
|
|
Juvenile Chronic Myelogenous Leukemia
|
Leukemia, Myelomonocytic, Juvenile
|
|
Juvenile Myelomonocytic Leukaemia Without Mention Of Remission
|
|
|
| Noonan Syndrome 1 |
|
Noonan Syndrome
|
NS1
|
|
Male Turner Syndrome
|
Female Pseudo-Turner Syndrome
|
|
Turner Phenotype With Normal Karyotype
|
Noonan Syndrome With Pigmented Villonodular Synovitis
|
|
Turner'S Phenotype, Karyotype Normal
|
Familial Turner Syndrome
|
|
Noonan'S Syndrome
|
Noonan-Ehmke Syndrome
|
|
Ns
|
Pseudo-Ullrich-Turner Syndrome
|
|
Turner Syndrome In Female With X Chromosome
|
Turner-Like Syndrome
|
|
Ullrich-Noonan Syndrome
|
Noonan-Like/Multiple Giant Cell Lesion Syndrome
|
|
Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions
|
Pterygium Colli Syndrome
|
|
Noonan Syndrome, Type 1
|
Turner Syndrome, Male
|
|
|
| Meningioma, Familial |
|
Meningioma
|
Familial Meningioma
|
|
Meningioma, Familial, Susceptibility To
|
Meningeal Neoplasm
|
|
Meningeal Neoplasms
|
Meningiomas
|
|
Meningioma, Nf2-Related, Somatic
|
Meningioma, Sis-Related
|
|
Meningothelial Cell Tumor
|
Neoplasm Of The Meninges
|
|
Primary Meningeal Tumor
|
Familial Multiple Meningioma
|
|
MNGMA
|
Meningioma, Benign, No Icd-O Subtype
|
|
Intracranial Meningioma
|
Meningothelial Cell Neoplasm
|
|
Supratentorial Meningioma
|
Primary Neoplasm Of Spinal Meninges
|
|
Benign Intracranial Meningioma
|
Benign Meningioma
|
|
Meningeal Tumours
|
Meningeal Sarcoma Of Unspecified Site
|
|
Meningothelial Sarcoma Of Unspecified Site
|
|
|
| Moyamoya Disease 1 |
|
Moyamoya Disease
|
Spontaneous Occlusion Of The Circle Of Willis
|
|
Mymy
|
Progressive Intracranial Arterial Occlusion
|
|
Moyamoya Syndrome
|
MYMY1
|
|
Cerebrovascular Moyamoya Disease
|
Moya-Moya Disease
|
|
Progressive Intracranial Occlusive Arteropathy
|
Idiopathic Moyamoya Disease
|
|
|
