| 疾病名称 |
别名 |
|
| Nephronophthisis 4 |
|
NPHP4
|
Juvenile Nephronophthisis 4
|
|
Nephronophthisis 4, Juvenile
|
Nephronophthisis, Type 4
|
|
|
| Senior-Loken Syndrome 4 |
|
SLSN4
|
Senior-Loken Syndrome, Type 4
|
|
|
| Juvenile Nephronophthisis |
|
Nephronophthisis
|
Nephronophthisis, Familial Juvenile
|
|
|
| Nephronophthisis |
|
Medullary Cystic Disease
|
Medullary Cystic Kidney
|
|
Nph
|
Nphp
|
|
Kidney Disease, Cystic, Medullary
|
|
|
| Senior-Loken Syndrome 1 |
|
Senior-Loken Syndrome
|
Renal Dysplasia And Retinal Aplasia
|
|
Renal-Retinal Syndrome
|
Loken-Senior Syndrome
|
|
Juvenile Nephronophthisis With Leber Amaurosis
|
SLSN1
|
|
Senior-Loken Syndrome-1
|
Loken Senior Syndrome
|
|
Senior Loken Syndrome
|
Renal Dysplasia Retinal Aplasia
|
|
Nephronophthisis With Retinal Dystrophy
|
Renal Dysplasia-Retinal Aplasia Syndrome
|
|
Slsn
|
|
|
| Infertility |
|
|
| Cogan Syndrome |
|
Cogan'S Syndrome
|
Diffuse Interstitual Keratitis
|
|
Cogans Syndrome
|
Oculovestibuloauditory Syndrome
|
|
|
| Nephronophthisis 2 |
|
NPHP2
|
Nph2
|
|
Nephronophthisis 2, Infantile
|
Infantile Nephronophthisis 2
|
|
Infantile Nephronophthisis
|
Nephronophthisis, Type 2
|
|
|
| Arima Syndrome |
|
Dekaban-Arima Syndrome
|
Joubert Syndrome With Bilateral Chorioretinal Coloboma
|
|
Cors
|
Cerebello-Oculo-Renal Syndrome
|
|
Cerebellooculorenal Syndrome
|
Js Type B
|
|
Js-Or
|
Joubert Syndrome 5
|
|
Joubert Syndrome With Senior-Loken Syndrome
|
Joubert Syndrome With Oculorenal Defect
|
|
Coloboma, Chorioretinal, With Cerebellar Vermis Aplasia
|
Cerebrooculohepatorenal Syndrome
|
|
Joubert Syndrome With Oculorenal Anomalies
|
Cerebro-Oculo-Hepato-Renal Syndrome
|
|
Chorioretinal Coloboma With Cerebellar Vermis Aplasia
|
Dekaban Arima Syndrome
|
|
Cor
|
Bj
|
|
Familial Aplasia Of The Vermis
|
|
|
| Nephronophthisis 1 |
|
NPHP1
|
Nephronophthisis, Familial Juvenile
|
|
Nph1
|
Nephronophthisis 1, Juvenile
|
|
Juvenile Nephronophthisis 1
|
Familial Juvenile Nephronophthisis 1
|
|
Nephronophthisis, Type 1
|
|
|
| Bardet-Biedl Syndrome |
|
Bbs
|
Biedl-Bardet Syndrome
|
|
|
| Cystic Kidney Disease |
|
Renal Cyst
|
Simple Renal Cyst
|
|
Kidney Cysts
|
Kidney Diseases, Cystic
|
|
Renal Cysts
|
Kidney Cyst
|
|
Cystic Kidney
|
Congenital Cystic Kidney Disease
|
|
Cystic Kidney Diseases
|
Bosniak 1 Cyst
|
|
|
| Cakut |
|
Renal Or Urinary Tract Malformation
|
Congenital Anomalies Of Kidney And Urinary Tract
|
|
Congenital Anomaly Of Kidney And Urinary Tract
|
Congenital Anomalies Of The Kidney And Urinary Tract
|
|
Kidney And Urinary Tract, Anomalies, Congenital
|
Renal Hypodysplasia, Nonsyndromic, 1
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
| Meckel Syndrome, Type 5 |
|
Meckel Syndrome 5
|
MKS5
|
|
Meckel-Gruber Syndrome, Type 5
|
|
|
| Joubert Syndrome 7 |
|
JBTS7
|
Cerebello-Oculo-Renal Syndrome 3
|
|
Cors3
|
Joubert Syndrome, Type 7
|
|
|
| Joubert Syndrome 20 |
|
JBTS20
|
Joubert Syndrome, Type 20
|
|
|
| Macular Degeneration, X-Linked Atrophic |
|
X-Linked Atrophic Macular Degeneration
|
Macular Degeneration, X-Linked, Atrophic
|
|
MDXLA
|
Degeneration, Macular, X-Linked Atrophic
|
|
|
| Nephronophthisis 14 |
|
Joubert Syndrome 19
|
NPHP14
|
|
JBTS19
|
Nephronophthisis, Type 14
|
|
|
| Meckel Syndrome, Type 2 |
|
MKS2
|
Meckel Syndrome 2
|
|
Meckel-Gruber Syndrome, Type 2
|
Meckel Syndrome Type 2
|
|
|
| Hydrolethalus Syndrome 1 |
|
Hydrolethalus Syndrome
|
HLS1
|
|
Salonen-Herva-Norio Syndrome
|
Hls
|
|
Hydrolethalus
|
Hydrolethalus Syndrome, Type 1
|
|
|
| Retinal Degeneration |
|
|
| Joubert Syndrome 14 |
|
JBTS14
|
Joubert Syndrome, Type 14
|
|
|
| Nephronophthisis 12 |
|
NPHP12
|
Joubert Syndrome 11
|
|
JBTS11
|
Nephronophthisis, Type 12
|
|
|
| Cone-Rod Dystrophy 2 |
|
Cone-Rod Dystrophy
|
CORD2
|
|
Cone-Rod Retinal Dystrophy
|
Rcrd2
|
|
Cone-Rod Retinal Dystrophy 2
|
Crd2
|
|
Cord
|
Crd
|
|
Retinal Cone-Rod Dystrophy
|
Cone-Rod Retinal Dystrophy-2
|
|
Retinal Cone-Rod Dystrophy 2
|
Tapetoretinal Degeneration
|
|
Cone-Rod Degeneration
|
Cone Rod Dystrophy
|
|
Dystrophy, Cone-Rod
|
Dystrophy, Cone-Rod, Type 2
|
|
Retinitis Pigmentosa
|
Retinitis Pigmentosa 2
|
|
Progressive Cone-Rod Dystrophy
|
|
|
| Renal-Hepatic-Pancreatic Dysplasia |
|
Ivemark'S Syndrome
|
Ivemark Ii Syndrome
|
|
Renohepaticopancreatic Dysplasia
|
|
|
| Retinitis Pigmentosa 77 |
|
RP77
|
Retinitis Pigmentosa, Type 77
|
|
|
| Male Infertility |
|
Infertility, Male
|
Infertility Male
|
|
Male Sterility
|
Absolute Infertility
|
|
|
| Renal Fibrosis |
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Nephronophthisis 19 |
|
NPHP19
|
Nephronophthisis, Type 19
|
|
|
| Meckel Syndrome, Type 8 |
|
Meckel Syndrome 8
|
MKS8
|
|
Meckel-Gruber Syndrome, Type 8
|
|
|
| Nephronophthisis 7 |
|
NPHP7
|
Nephronophthisis, Type 7
|
|
|
| Asphyxiating Thoracic Dystrophy |
|
Jeune Thoracic Dystrophy
|
Jeune Syndrome
|
|
Asphyxiating Thoracic Dysplasia
|
Short-Rib Thoracic Dysplasia With Or Without Polydactyly
|
|
Thoracic Pelvic Phalangeal Dystrophy
|
Asphyxiating Thoracic Chondrodystrophy
|
|
Atd
|
Chondroectodermal Dysplasia-Like Syndrome
|
|
Infantile Thoracic Dystrophy
|
Jeune Thoracic Dysplasia
|
|
Thoracic Asphyxiant Dystrophy
|
Thoracic-Pelvic-Phalangeal Dystrophy
|
|
Short-Rib Thoracic Dysplasia Without Polydactyly
|
Asphyxiating Thoracic Dystrophy Of The Newborn
|
|
Asphyxiating Thorax Dystrophy
|
|
|
| Cone-Rod Dystrophy 1 |
|
CORD1
|
Crd1
|
|
Cone-Rod Retinal Dystrophy-1
|
Retinitis Pigmentosa 1
|
|
|
| Retinitis Pigmentosa 69 |
|
RP69
|
Retinitis Pigmentosa, Type 69
|
|
|
| End Stage Renal Disease |
|
End Stage Renal Failure
|
End-Stage Kidney Disease
|
|
Kidney Failure, Chronic
|
Chronic Kidney Disease Stage 5
|
|
|
| Nephronophthisis 9 |
|
NPHP9
|
Nephronophthisis, Type 9
|
|
|
| Cholestasis, Benign Recurrent Intrahepatic, 2 |
|
BRIC2
|
Benign Recurrent Intrahepatic Cholestasis 2
|
|
Benign Recurrent Intrahepatic Cholestasis Type 2
|
Bric Type 2
|
|
Cholestasis, Intrahepatic, Recurrent, Benign, Type 2
|
Cholestasis, Benign Recurrent Intrahepatic 2
|
|
|
| Cone-Rod Dystrophy 13 |
|
CORD13
|
Dystrophy, Cone-Rod, Type 13
|
|
|
| Kidney Disease |
|
Renal Failure
|
Kidney Failure
|
|
Kidney Diseases
|
Nephropathy
|
|
Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
|
Renal Anomaly
|
Kidney Dysfunction
|
|
Renal Disease
|
Nephropathies
|
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
|
| 3-Methylcrotonyl-Coa Carboxylase 2 Deficiency |
|
MCC2D
|
Mcc2 Deficiency
|
|
3-Methylcrotonyl Coa Carboxylase 2 Deficiency
|
3-Methylcrotonylglycinuria Ii
|
|
Methylcrotonylglycinuria, Type Ii
|
3-Methylcrotonoyl-Coa Carboxylase 2 Deficiency
|
|
3-Methylcrotonylglycinuria Type Ii
|
Mcgii
|
|
Methylcrotonylglycinuria Type Ii
|
|
|
| Nephronophthisis 11 |
|
NPHP11
|
Nephronophthisis, Type 11
|
|
|
| Meckel Syndrome, Type 1 |
|
Meckel-Gruber Syndrome
|
Meckel Syndrome
|
|
Dysencephalia Splanchnocystica
|
Meckel Syndrome 1
|
|
MKS1
|
Mks
|
|
Gruber Syndrome
|
Meckel-Gruber Syndrome, Type 1
|
|
Mes
|
Dysencephalia Splachnocystica
|
|
Meckel Gruber Syndrome
|
Meckel Syndrome Type 1
|
|
|
| Nephronophthisis 18 |
|
NPHP18
|
Nephronophthisis, Type 18
|
|
|
| Coach Syndrome 1 |
|
Coach Syndrome
|
Joubert Syndrome With Congenital Hepatic Fibrosis
|
|
Gentile Syndrome
|
Joubert Syndrome With Hepatic Defect
|
|
Js-H
|
COACH1
|
|
Cerebellar Vermis Hypo/Aplasia, Oligophrenia, Congenital Ataxia, Ocular Coloboma, And Hepatic Fibrosis
|
Cerebellar Vermis Hypoplasia-Oligophrenia-Congenital Ataxia-Coloboma-Hepatic Fibrosis
|
|
Cerebellar Vermis Hypo/Aplasia, Oligophrenia, Ataxia Congenital, Coloboma, And Hepatic Fibrosis
|
Cerebellar Vermis Hypo/Aplasia Oligophrenia Congenital Ataxia Ocular Coloboma And Hepatic Fibrosis
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Joubert Syndrome 1 |
|
Joubert Syndrome
|
Jbts
|
|
Cerebellooculorenal Syndrome 1
|
JBTS1
|
|
Joubert-Boltshauser Syndrome
|
Cerebelloparenchymal Disorder Iv
|
|
Cpd4
|
Cors1
|
|
Joubert Syndrome And Related Disorders
|
Jsrd
|
|
Familial Aplasia Of The Vermis
|
Joubert Syndrome Related Disorders
|
|
Js
|
Cerebellar Vermis Agenesis
|
|
Cerebelloparenchymal Disorder 4
|
Agenesis Of Cerebellar Vermis
|
|
Cerebello-Oculo-Renal Syndrome
|
Cors
|
|
Joubert-Bolthauser Syndrome
|
Cpd Iv
|
|
Classic Joubert Syndrome
|
Joubert Syndrome Type A
|
|
Pure Joubert Syndrome
|
Cerebello-Oculo-Renal Syndrome 1
|
|
Joubert Syndrome-1
|
Joubert Syndrome, Type 1
|
|
Joubert'S Syndrome
|
|
|
| Joubert Syndrome 21 |
|
JBTS21
|
Joubert Syndrome, Type 21
|
|
|
| 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
|
|
|
| Hydrocephalus |
|
Hydrocephalus, Nonsyndromic, Autosomal Recessive
|
Hydrocephalus, X-Linked
|
|
Hydrocephalus Adverse Event
|
Hydrocephaly Nos
|
|
|
| Joubert Syndrome 3 |
|
JBTS3
|
Joubert Syndrome With Ocular Defect
|
|
Joubert Syndrome With Ocular Anomalies
|
Js-O
|
|
Joubert Syndrome With Retinopathy
|
Joubert Syndrome-3
|
|
Joubert Syndrome, Type 3
|
|
|
| Joubert Syndrome 5 |
|
JBTS5
|
Joubert Syndrome, Type 5
|
|
|
| Polycystic Liver Disease 1 With Or Without Kidney Cysts |
|
Polycystic Liver Disease 1
|
PCLD1
|
|
Cyst
|
Liver Disease, Polycystic, Type 1
|
|
Polycystic Liver Disease
|
|
|
| Orofaciodigital Syndrome Vi |
|
OFD6
|
Varadi-Papp Syndrome
|
|
Varadi Syndrome
|
Joubert Syndrome With Orofaciodigital Defect
|
|
Orofaciodigital Syndrome Type 6
|
Orofaciodigital Syndrome 6
|
|
Oral-Facial-Digital Syndrome, Type Vi
|
Ofds Vi
|
|
Polydactyly, Cleft Lip/Palate Or Lingual Lump, And Psychomotor Retardation
|
Polydactyly Cleft Lip Palate Psychomotor Retardation
|
|
Oral-Facial-Digital Syndrome Type 6
|
Polydactyly-Cleft Lip/Palate-Psychomotor Retardation Syndrome
|
|
Polydactyly - Cleft Lip/Palate - Psychomotor Retardation
|
Váradi Syndrome
|
|
Váradi-Papp Syndrome
|
Joubert Syndrome With Oral-Facial-Digital Syndrome
|
|
Oral-Facial-Digital Syndrome 6
|
Joubert-Orofaciodigital Syndrome
|
|
Orofaciodigital Syndrome, Type Vi
|
|
|
| Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease |
|
Autosomal Recessive Polycystic Kidney Disease
|
Arpkd
|
|
Polycystic Kidney Disease, Autosomal Recessive
|
Polycystic Kidney And Hepatic Disease 1
|
|
Pkhd1
|
PKD4
|
|
Polycystic Kidney Disease 4 With Or Without Hepatic Disease
|
Polycystic Kidney Disease, Infantile, Type I
|
|
Polycystic Kidney Disease, Infantile Type
|
Polycystic Kidney, Autosomal Recessive
|
|
Pkd3, Formerly
|
Polycystic Kidney Disease 4, With Or Without Hepatic Disease
|
|
Arpkd/Chf
|
Ar-Pkd
|
|
Polycystic Kidney Disease 4, With Or Without Polycystic Liver Disease
|
Infantile Polycystic Kidney Disease Type I
|
|
Pkd3
|
Kidney, Polycystic, Disease, Type 4, With/Without Hepatic Disease
|
|
Polycystic Kidney Disease 3, Autosomal Dominant
|
|
|
| Cranioectodermal Dysplasia |
|
Sensenbrenner Syndrome
|
Levin Syndrome 1
|
|
Ced
|
Levin Syndrome
|
|
Dysplasia, Cranioectodermal
|
|
|
| Visceral Heterotaxy |
|
Situs Ambiguus
|
Heterotaxia
|
|
Heterotaxy Syndrome
|
Heterotaxy
|
|
Lateralization Defect
|
Situs Ambiguous
|
|
Left Isomerism
|
Htx
|
|
Ivemark Syndrome
|
Right Isomerism
|
|
Situs Ambiguus Viscerum
|
Incomplete Situs Inversus
|
|
Partial Situs Inversus
|
Heterotaxy, Visceral
|
|
Asplenia Syndrome
|
Bilateral Left-Sidedness
|
|
Polysplenia Syndrome
|
Moller Syndrome
|
|
|
| Leber Plus Disease |
|
Leber Congenital Amaurosis
|
Lca
|
|
Leber'S Amaurosis
|
Leber'S Disease
|
|
Amaurosis Congenita Of Leber
|
Amaurosis Congenita Of Leber, Type 1
|
|
Lhon Plus Disease
|
Congenital Absence Of The Rods And Cones
|
|
Congenital Retinal Blindness
|
Crb
|
|
Congenital Amaurosis Of Retinal Origin
|
Leber'S Congenital Amaurosis
|
|
Leber Congenital Amaurosis 1
|
Leber'S Congenital Tapetoretinal Degeneration
|
|
Leber'S Congenital Tapetoretinal Dysplasia
|
Lca1
|
|
Leber Congenital Amaurosis Type 1
|
Retinal Blindness, Congenital
|
|
Amaurosis, Leber Congenital
|
Dysgenesis Neuroepithelialis Retinae
|
|
Hereditary Epithelial Dysplasia Of Retina
|
Hereditary Retinal Aplasia
|
|
Heredoretinopathia Congenitalis
|
Leber Abiotrophy
|
|
Leber Congenital Tapetoretinal Degeneration
|
Lebers Congenital Amaurosis
|
|
Optic Atrophy, Hereditary, Leber
|
|
|
| Situs Inversus |
|
Situs Inversus Viscerum
|
Laterality Sequence
|
|
Complete Transposition
|
Siv
|
|
|
| Autosomal Dominant Polycystic Kidney Disease |
|
Polycystic Kidney Disease, Adult Type
|
Adpkd
|
|
Polycystic Kidney Diseases
|
Polycystic Kidney, Autosomal Dominant
|
|
Congenital Biliary Ectasias
|
Polycystic Kidney And Hepatic Disease 1
|
|
Polycystic Kidney Disease, Autosomal Dominant
|
Kidney, Polycystic, Disease, Autosomal Dominant
|
|
Adult Polycystic Kidney Disease
|
Polycystic Kidney, Adult Type
|
|
Apckd - [Autosomal Polycystic Kidney Disease]
|
|
|
| Coloboma Of Macula |
|
Coloboma
|
Congenital Ocular Coloboma
|
|
Microphthalmia, Isolated, With Coloboma
|
Agenesis Of Macula
|
|
Hereditary Macular Coloboma
|
Ocular Coloboma
|
|
Coloboma Of Eye
|
Macular Coloboma
|
|
Uveoretinal Coloboma
|
|
|
| Polycystic Kidney Disease |
|
Polycystic Kidney Diseases
|
Pkd
|
|
Polycystic Renal Disease
|
Kidney Disease, Polycystic
|
|
Polycystic Kidney, Autosomal Dominant
|
|
|
| Primary Ciliary Dyskinesia |
|
Immotile Cilia Syndrome
|
Kartagener Syndrome
|
|
Dextrocardia Bronchiectasis And Sinusitis
|
Pcd
|
|
Ciliary Motility Disorders
|
Ciliary Motility Disorder
|
|
Immotile Ciliary Syndrome
|
Ciliary Dyskinesia Primary
|
|
Ics
|
Polynesian Bronchiectasis
|
|
Dextrocardia-Bronchiectasis-Sinusitis Syndrome
|
Immotile Cilia Syndrome, Kartagener Type
|
|
Primary Ciliary Dyskinesia And Situs Inversus
|
Primary Ciliary Dyskinesia, Kartagener Type
|
|
Siewert Syndrome
|
Dyskinesia, Ciliary, Primary
|
|
|
