| 疾病名称 |
别名 |
|
| Lesch-Nyhan Syndrome |
|
Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency
|
LNS
|
|
Hprt Deficiency
|
Complete Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency
|
|
Hypoxanthine Guanine Phosphoribosyltransferase Deficiency
|
X-Linked Hyperuricemia
|
|
Choreoathetosis Self-Mutilation Syndrome
|
Hprt1 Deficiency
|
|
Hprt Deficiency, Complete
|
Deficiency Of Imp Pyrophosphorylase
|
|
Hgprt Deficiency
|
Lesch-Nyhan Disease
|
|
Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency
|
Hg-Prt Deficiency
|
|
Hypoxanthine-Guanine-Phosphoribosyltransferase Deficiency
|
Lesch - Nyhan Syndrome
|
|
Hprt1 Disorders
|
Lesch Nyhan Syndrome
|
|
Complete Hprt Deficiency Complete
|
Lesch Nyhan Disease
|
|
Complete Hprt Deficiency
|
Deficiency Of Guanine Phosphoribosyltransferase
|
|
Deficiency Of Hypoxanthine Phosphoribosyltransferase
|
Hypoxanthine Phosphoribosyltransferase Deficiency
|
|
Juvenile Gout, Choreoathetosis, Mental Retardation Syndrome
|
Juvenile Hyperuricemia Syndrome
|
|
Lnd
|
Primary Hyperuricemia Syndrome
|
|
Total Hprt Deficiency
|
Total Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency
|
|
X-Linked Primary Hyperuricemia
|
X-Linked Uric Aciduria Enzyme Defect
|
|
Hprt Complete Deficiency
|
Hprt Deficiency Grade Iv
|
|
Hypoxanthine Guanine Phosphoribosyltransferase Complete Deficiency
|
Hypoxanthine Guanine Phosphoribosyltransferase Deficiency, Grade Iv
|
|
Hypoxanthine-Guanine Phosphoribosyltransferase 1 Deficiency
|
Hprt - [ Hypoxanthine-Guanine Phosphoribosyltransferase] Complete Deficiency
|
|
Total Hgprt - [Hypoxanthine-Guanine Phosphoribosyltransferase] Deficiency
|
|
|
| Hyperuricemia, Hprt-Related |
|
Hprt-Related Gout
|
Kelley-Seegmiller Syndrome
|
|
Hprt Deficiency, Partial
|
HRH
|
|
Gout, Hprt-Related
|
Hprt1 Deficiency, Partial
|
|
Hrpt-Related Hyperuricemia
|
Hprt Deficiency, Grade I
|
|
Hprt Partial Deficiency
|
Hprt-Related Hyperuricemia
|
|
Hprt1 Partial Deficiency
|
Hypoxanthine Guanine Phosphoribosyltransferase 1 Partial Deficiency
|
|
Hypoxanthine Guanine Phosphoribosyltransferase Deficiency, Grade I
|
Hypoxanthine Guanine Phosphoribosyltransferase Partial Deficiency
|
|
Partial Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency
|
Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency, Partial
|
|
Hyperuricemia, Hrpt-Related
|
|
|
| Gout |
|
Gouty Arthritis
|
Articular Gout
|
|
Gouty Arthropathy
|
Arthritis, Gouty
|
|
Arthritis Gouty
|
Idiopathic Gout
|
|
Idiopathic Gout, Unspecified Site
|
Gouty Bursitis
|
|
Uratic Arthritis
|
Gout Nos
|
|
Gouty
|
Gouty Diathesis
|
|
|
| Hyperuricemia |
|
Blood Urate Raized
|
Uricacidemia
|
|
|
| Nephrolithiasis, Uric Acid |
|
Nephrolithiasis, Uric Acid, Susceptibility To
|
Uric Acid Urolithiasis
|
|
Uric Acid Nephrolithiasis
|
UAN
|
|
Acute Urate Nephropathy
|
Urolithiasis, Uric Acid
|
|
Urolithiasis, Uric Acid, Susceptibility To
|
Uric Acid Renal Calculus
|
|
|
| Phosphoribosylpyrophosphate Synthetase Superactivity |
|
PRPS1 SUPERACTIVITY
|
Prpp Synthetase Superactivity
|
|
Gout, Prps-Related
|
Prpp Synthetase Deficiency
|
|
Prpp Synthetase Overactivity
|
Prs Overactivity
|
|
Prs Superactivity
|
Mild Phosphoribosylpyrophosphate Synthetase Superactivity
|
|
Mild Prpp Synthetase Superactivity
|
Mild Prps1 Superactivity
|
|
Severe Phosphoribosylpyrophosphate Synthetase Superactivity
|
Severe Prpp Synthetase Superactivity
|
|
Severe Prps1 Superactivity
|
Prps-Related Gout
|
|
Superactivity, Phosphoribosylpyrophosphate Synthetase
|
|
|
| Purine-Pyrimidine Metabolic Disorder |
|
Inborn Errors Of Purine-Pyrimidine Metabolism
|
Disorder Of Purine Or Pyrimidine Metabolism
|
|
|
| Tubulointerstitial Kidney Disease, Autosomal Dominant, 1 |
|
Familial Juvenile Hyperuricemic Nephropathy
|
Mckd2
|
|
Familial Juvenile Hyperuricemic Nephropathy Type 1
|
Fjhn
|
|
Medullary Cystic Kidney Disease 2
|
Uromodulin-Associated Kidney Disease
|
|
Medullary Cystic Kidney Disease Type 2
|
ADTKD1
|
|
Hnfj1
|
Glomerulocystic Kidney Disease With Hyperuricemia And Isosthenuria
|
|
Adtkd-Umod
|
Familial Juvenile Hyperuricemic Nephropathy 1
|
|
Umod-Related Adtkd
|
Umod-Related Autosomal Dominant Tubulointerstitial Kidney Disease
|
|
Hyperuricemic Nephropathy, Familial Juvenile, 1
|
Gouty Nephropathy, Familial Juvenile
|
|
Medullary Cystic Kidney Disease 2, Autosomal Dominant
|
Admckd2
|
|
Autosomal Dominant Tubulointerstitial Kidney Disease Due To Umod Mutations
|
Adtkd Due To Umod Mutations
|
|
Autosomal Dominant Tubulointerstitial Kidney Disease, Umod-Related
|
Autosomal Dominant Medullary Cystic Kidney Disease Type 2
|
|
Umod-Associated Kidney Disease
|
Uromodulin Kidney Disease
|
|
Familial Gout-Kidney Disease
|
Familial Gouty Nephropathy
|
|
Umak
|
Umod-Related Kidney Disease
|
|
Uromodulin Storage Disease
|
Fjhn1
|
|
Gouty Nephropathy Familial Juvenile
|
Nephropathy Familial With Gout
|
|
Hyperuricemic Nephropathy, Familial Juvenile 1
|
Hyperuricemic Nephropathy, Familial Juvenile
|
|
Kidney Disease, Glomerulocystic, With Hyperuricemia And Isosthenuria
|
Nephropathy, Hyperuricemic, Juvenile, Familial, Type 1
|
|
Kidney Disease, Cystic, Medullary, Type 2
|
Medullary Cystic Kidney Disease Type Ii
|
|
Familial Juvenile Gout
|
|
|
| Disorder Of Purine Metabolism |
|
Purine Metabolism Disorder
|
|
|
| Cockayne Syndrome |
|
Cockayne'S Syndrome
|
Dwarfism-Retinal Atrophy-Deafness Syndrome
|
|
Neill-Dingwall Syndrome
|
Progeria-Like Syndrome
|
|
Progeroid Nanism
|
Cs
|
|
|
| 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
|
|
|
| Nephrolithiasis |
|
Kidney Stones
|
Stone - Kidney/Ureter
|
|
Kidney Calculi
|
|
|
| Hypouricemia, Renal, 1 |
|
Dalmatian Hypouricemia
|
Renal Hypouricemia
|
|
Hypouricemia, Renal
|
Familial Renal Hypouricemia
|
|
RHUC1
|
Hereditary Renal Hypouricemia
|
|
Familial Renal Hypouricaemia
|
Rhuc
|
|
Hypouricemia Renal 1
|
Hypouricemia, Renal, Type 1
|
|
|
| Xeroderma Pigmentosum, Variant Type |
|
Xeroderma Pigmentosum
|
XPV
|
|
Xeroderma Pigmentosum Variant Type
|
Xeroderma Pigmentosum With Normal Dna Repair Rates
|
|
Photosensitivity With Defective Dna Synthesis
|
Xp
|
|
De Sanctis-Cacchione Syndrome
|
Desanctis-Cacchione Syndrome
|
|
Xeroderma Pigmentosa
|
Xerodermic Idiocy
|
|
Xeroderma Pigmentosum Variant
|
Xp - [Xeroderma Pigmentosum]
|
|
Atrophoderma Pigmentosum
|
|
|
| Teratocarcinoma |
|
Mixed Embryonal Carcinoma And Teratoma
|
|
|
| Urolithiasis |
|
|
| 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
|
|
|
| Incontinentia Pigmenti |
|
Bloch-Sulzberger Syndrome
|
IP
|
|
Incontinentia Pigmenti, Familial Male-Lethal Type
|
Incontinentia Pigmenti Syndrome
|
|
Bloch-Siemens Syndrome
|
Ip2
|
|
Incontinentia Pigmenti, Type Ii, Formerly
|
Ip2, Formerly
|
|
Incontinentia Pigmenti Type 2
|
Bloch-Siemens-Sulzberger Syndrome
|
|
Familial Incontinentia Pigmenti Male-Lethal Type
|
Familial Incontinentia Pigmenti Type Ii
|
|
Incontinentia Pigmenti, Type Ii
|
Bloch Sulzberger Syndrome
|
|
Incontinentia Pigmenti Achromians
|
Incontinentia Pigmenti Of Bloch-Sulzberger
|
|
Nevus Pigmentosus Systematicus
|
|
|
| Adenine Phosphoribosyltransferase Deficiency |
|
Aprt Deficiency
|
2,8-Dihydroxyadenine Urolithiasis
|
|
APRTD
|
2,8-Dihydroxyadeninuria
|
|
Dihydroxyadeninuria
|
Urolithiasis, 2,8-Dihydroxyadenine
|
|
Urolithiasis, Dha
|
Nephrolithiasis, Dha
|
|
Dha Crystalline Nephropathy
|
Nephrolithiasis Dha
|
|
Urolithiasis Dha
|
|
|
| Immunodeficiency With Hyper-Igm, Type 1 |
|
Immunodeficiency, X-Linked, With Hyper-Igm
|
Hyper Igm Syndrome
|
|
HIGM1
|
Xhim
|
|
Hyper-Igm Syndrome
|
Higm
|
|
Hyper-Igm Syndrome 1
|
Immunodeficiency 3
|
|
Imd3
|
Immunodeficiency With Hyper-Igm
|
|
Immunodeficiency With Hyper Igm Type 1
|
Ihis
|
|
X-Linked Hyper Igm Syndrome
|
Hyper-Igm Immunodeficiency, X-Linked
|
|
Hyper Igm Immunodeficiency, X-Linked
|
Hyper Igm Syndrome 1
|
|
X-Linked Immunodeficiency With Hyper-Igm 1
|
Immunodeficiency, With Hyper Igm
|
|
Immunodeficiency, With Hyper Igm, Type 1
|
Hyper-Igm Immunodeficiency Syndrome, Type 1
|
|
Hyperimmunoglobulin M Syndrome
|
|
|
| Paroxysmal Nocturnal Hemoglobinuria |
|
Marchiafava-Micheli Disease
|
Pnh
|
|
Hemoglobinuria, Paroxysmal
|
Marchiafava-Micheli Syndrome
|
|
Paroxysmal Hemoglobinuria Nocturnal
|
Nocturnal Haemoglobinuria
|
|
Nocturnal Paroxysmal Haematuria
|
Nocturnal Paroxysmal Haemoglobinaemia
|
|
|
| Purine Nucleoside Phosphorylase Deficiency |
|
Purine-Nucleoside Phosphorylase Deficiency
|
Pnp Deficiency
|
|
Nucleoside Phosphorylase Deficiency
|
Immunodeficiency Due To Purine Nucleoside Phosphorylase Deficiency
|
|
Deficiency Of Inosine Phosphorylase
|
Pnpase Deficiency
|
|
PNPD
|
|
|
| Connective Tissue Disease |
|
Connective Tissue Diseases
|
Connective Tissue Disorder
|
|
Abnormality Of Connective Tissue
|
Disorder Of Connective Tissue
|
|
Connective Tissue Disorders
|
|
|
| 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
|
|
|
| Xanthinuria |
|
Xanthine Dehydrogenase Deficiency
|
Xanthine Oxidase Deficiency
|
|
Hereditary Xanthinuria
|
Xanthic Urolithiasis
|
|
Xanthine Stone Disease
|
Xanthinuria, Type I
|
|
Combined Deficiency Of Xanthine Dehydrogenase And Aldehyde Oxidase
|
Xdh Deficiency
|
|
Classic Xanthinuria
|
Xanthinuria, Type Ii
|
|
Classical Xanthinuria
|
Xanthine Calculus
|
|
|
| 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
|
|
|
| Fragile X Syndrome |
|
FXS
|
Martin-Bell Syndrome
|
|
Fraxa Syndrome
|
Marker X Syndrome
|
|
X-Linked Mental Retardation And Macroorchidism
|
Fragile X Mental Retardation Syndrome
|
|
Fra Syndrome
|
Mental Retardation, X-Linked, Associated With Marxq28
|
|
X-Linked Intellectual Disability And Macroorchidism
|
Frax Syndrome
|
|
Symptomatic Form Of Fragile X Syndrome In Female Carriers
|
Fragile-X Syndrome
|
|
Fraxe Syndrome
|
|
|
| Arts Syndrome |
|
ARTS
|
Mrxsarts
|
|
Ataxia, Fatal X-Linked, With Deafness And Loss Of Vision
|
Mrxs18
|
|
Lethal Ataxia With Deafness And Optic Atrophy
|
Fatal X-Linked Ataxia With Deafness And Loss Of Vision
|
|
Mental Retardation, X-Linked, Syndromic, Arts Type
|
Mental Retardation, X-Linked, Syndromic 18
|
|
Syndromic X-Linked Mental Retardation 18
|
Syndromic X-Linked Mental Retardation Arts Type
|
|
Lethal Ataxia-Deafness-Optic Atrophy
|
X-Linked Fatal Ataxia With Deafness And Loss Of Vision
|
|
Ataxia-Deafness-Optic Atrophy, Lethal
|
Lethal Ataxia With Hearing Loss And Optic Atrophy
|
|
Art
|
|
|
| Deafness, Autosomal Recessive 40 |
|
DFNB40
|
Autosomal Recessive Nonsyndromic Deafness 40
|
|
Autosomal Recessive Deafness 40
|
|
|
| Deafness, Autosomal Recessive 55 |
|
DFNB55
|
Autosomal Recessive Nonsyndromic Deafness 55
|
|
Autosomal Recessive Deafness 55
|
|
|
| Dissociated Nystagmus |
|
|
| Rett Syndrome |
|
Atypical Rett Syndrome
|
RTT
|
|
Rett Disorder
|
Rts
|
|
Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use
|
Rett Syndrome, Preserved Speech Variant
|
|
Rett Syndrome, Atypical
|
Rett'S Disorder
|
|
Rett Syndrome Variant
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome
|
|
Cerebroatrophic Hyperammonemia
|
Rett Like Syndrome
|
|
Rett'S Syndrome
|
Atypical Rtt
|
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use
|
Rett Syndrome Preserved Speech Variant
|
|
Rett Syndrome Zappella Variant
|
Rett Syndrome, Zappella Variant
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Dystonia |
|
Dystonic Disease
|
Dystonic Disorder
|
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|
| Inflammatory Bowel Disease 16 |
|
IBD16
|
Inflammatory Bowel Disease 16, Susceptibility To
|
|
|
| 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
|
|
|
| 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
|
|
|
| Leukemia, Acute Lymphoblastic |
|
Acute Lymphoblastic Leukemia
|
ALL
|
|
Acute Lymphocytic Leukemia
|
Leukemia, Acute Lymphocytic, Susceptibility To, 1
|
|
Acute Lymphoblastic Leukaemia
|
Precursor Lymphoblastic Lymphoma/Leukemia
|
|
Precursor Lymphoid Neoplasm
|
Leukemia, Acute Lymphoblastic, Susceptibility To
|
|
B-Cell Acute Lymphoblastic Leukemia
|
Leukemia, Acute Lymphocytic 1
|
|
Acute Lymphocytic Leukaemia
|
Acute Lymphoblastic Leukemia/Lymphoma
|
|
All1
|
Childhood Acute Lymphoblastic Leukemia
|
|
Leukemia Acute Lymphoblastic 1
|
Leukemia Acute Lymphoblastic B-Hyperdiploid
|
|
Leukemia Acute Lymphocytic
|
Leukemia Acute Lymphocytic 1
|
|
Leukemia B-Cell Acute Lymphoblastic
|
Leukemia T-Cell Acute Lymphoblastic
|
|
Leukemia, Acute Lymphoblastic, 3
|
ALL3
|
|
Lymphoblastic Leukemia Acute
|
Leukemia, Acute, Lymphoblastic
|
|
Precursor Cell Lymphoblastic Leukemia Lymphoma
|
Leukemia, Lymphocytic, Acute, L1
|
|
Leukemia, Acute Lymphoblastic, Susceptibility To, 3
|
|
|
| Systemic Lupus Erythematosus |
|
Lupus Nephritis
|
SLE
|
|
Disseminated Lupus Erythematosus
|
Systemic Lupus Erythematosus, Susceptibility To
|
|
Lupus Erythematosus, Systemic
|
Lupus Nephritis, Susceptibility To
|
|
Libman-Sacks Disease
|
Systemic Lupus Erythematosus Susceptibility To
|
|
Sle - Lupus Erythematosus, Systemic
|
Le Syndrome
|
|
Lupus
|
Lupus Erythematosus Systemic
|
|
Lupus Erythematosus, Systemic, Susceptibility To
|
Lupus Vulgaris
|
|
Lupus Erythematosus, Discoid
|
Lupus Erythematosus
|
|
Systemic Lupus Erythematosus Nos
|
Sle - [Systemic Lupus Erythematosus]
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Syndromic Intellectual Disability |
|
|
| Alzheimer Disease, Familial, 1 |
|
Alzheimer Disease
|
Alzheimer'S Disease
|
|
Presenile And Senile Dementia
|
AD1
|
|
Alzheimer Disease, Susceptibility To
|
Alzheimer Disease, Late-Onset, Susceptibility To
|
|
Alzheimer Disease 1, Familial
|
AD
|
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
|
Alzheimers Dementia
|
Alzheimer Dementia
|
|
Alzheimer Sclerosis
|
Alzheimer Syndrome
|
|
Alzheimer-Type Dementia
|
Dat
|
|
Primary Senile Degenerative Dementia
|
Sdat
|
|
Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
|
Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
|
Dementia Due To Alzheimer'S Disease
|
Alzheimer Disease Type 1
|
|
Alzheimers
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
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Pericentral Pigmentary Retinopathy
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Pigmentary Retinopathy
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Tapetoretinal Degeneration
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Rcd
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Retinitis Pigmentosa Autosomal Recessive
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ARRP
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Retinitis Pigmentosa, Autosomal Recessive
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Retinitis Pigmentosa 1
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