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Ontology Browser

Term:
Nephrosis with Deafness and Urinary Tract and Digital Malformations (DOID:9007942)
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Parent Terms Term With Siblings Child Terms
Deafness +     
nephrosis +     
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
Aase Smith Syndrome 
Abruzzo-Erickson syndrome  
Absence of Tibia with Congenital Deafness 
acrocardiofacial syndrome 
Acromegaloid Facial Appearance Syndrome 
acromesomelic dysplasia-3  
acromicric dysplasia +   
Acropectoral Syndrome 
Adams-Oliver syndrome +   
ADULT syndrome  
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Albinism Deafness Syndrome 
Alport syndrome +   
Antley-Bixler syndrome with disordered steroidogenesis  
Arachnodactyly +   
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
Atelosteogenesis Type 3  
Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects 
autosomal dominant congenital deafness with onychodystrophy  
autosomal dominant nonsyndromic deafness 65  
Ayazi Syndrome 
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations  
Bagatelle Cassidy Syndrome 
Beaulieu-Boycott-Innes Syndrome  
Bifid or Double Ureter 
blepharophimosis, ptosis, and epicanthus inversus syndrome +   
brachydactyly +   
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome 
Brachyolmia Type 1, Hobaek Type 
Branchiogenic-Deafness Syndrome 
Burn-McKeown syndrome  
Calabro Syndrome 
Camptobrachydactyly 
Cardiac-Urogenital Syndrome  
Cardioacrofacial Dysplasia +   
Cardioauditory Syndrome of Sanchez Cascos 
Cartwright Nelson Fryns Syndrome 
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula 
CHILD syndrome  
CHITAYAT SYNDROME  
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
congenital limbs-face contractures-hypotonia-developmental delay syndrome  
Congenital Myopathy with Neuropathy and Deafness  
Congenital Upper Extremity Deformities +   
corpus callosum agenesis-abnormal genitalia syndrome  
Coxoauricular Syndrome 
Craniomicromelic Syndrome 
Daentl Towsend Siegel Syndrome 
Davenport Donlan Syndrome 
Deaf-Blind Disorders +   
Deafness Hyperuricemia Neurologic Ataxia 
Deafness with Anhidrotic Ectodermal Dysplasia 
Deafness, Autosomal Dominant, due to Mutation In Myo1a 
DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY  
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
Deafness, Congenital Onychodystrophy, Recessive Form 
DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY  
Deafness, Nephritis, Anorectal Malformation 
Deafness, with Smith-Magenis Syndrome  
Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull 
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
disorder of sexual development +   
Distal Transverse Limb Defects with Mental Retardation and Spasticity 
DK Phocomelia Syndrome 
Duker Weiss Siber syndrome 
Ectrodactyly-Polydactyly 
Ectromelia +   
ENDOVE SYNDROME, LIMB-BRAIN TYPE  
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
Epispadias +   
Feingold syndrome +   
fetal akinesia deformation sequence syndrome X-linked 
fetal encasement syndrome  
Fine-Lubinsky Syndrome  
Forsythe-Wakeling Syndrome 
Fountain Syndrome 
Fraser syndrome +   
Freire-Maia Odontotrichomelic Syndrome 
Fryns Syndrome  
Fused Kidney  
Galloway-Mowat syndrome +   
Genitopatellar Syndrome  
GENITOURINARY AND/OR BRAIN MALFORMATION SYNDROME  
Grubben de Cock Borghgraef Syndrome 
Hand and Foot Deformity with Flat Facies 
hand-foot-genital syndrome  
Hanhart Syndrome 
Heart Defects Limb Shortening 
hereditary spastic paraplegia 24 
Herrmann Syndrome 
high myopia-sensorineural deafness syndrome  
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hyperlipoproteinemia Type II, and Deafness 
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
hypochondroplasia  
Hypoglossia-Hypodactylia 
Hypokalemic Tubulopathy and Deafness  
hypoparathyroidism-deafness-renal disease syndrome  
hypospadias +   
Ichthyosis Tapered Fingers Midline Groove Up 
IMAGe syndrome  
IMAGEI Syndrome  
Intellectual Developmental Disorder with Dysmorphic Facies, Seizures, and Distal Limb Anomalies  
ITM2B-related cerebral amyloid angiopathy 2  
Johnson Neuroectodermal Syndrome 
Jones Syndrome 
Kaplan Plauchu Fitch Syndrome 
Kaufman oculocerebrofacial syndrome  
Keipert syndrome  
Keratitis-Ichthyosis-Deafness Syndrome +   
Konigsmark Knox Hussels Syndrome 
Kuster Syndrome 
Laryngeal Atresia, Encephalocele, and Limb Deformities 
Le Marec Bracq Picaud Syndrome 
Lethal Congenital Nonspherocytic Hemolytic Anemia with Genital and Other Abnormalities 
Lethal Faciocardiomelic Dysplasia 
LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS  
Limb-Mammary Syndrome  
lipoid nephrosis  
Lower Extremity Deformities, Congenital +   
Lynch Lee Murday syndrome 
Malformation of Arms 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Megalodactyly  
Mental Retardation Spasticity Ectrodactyly 
Mesomelia-Synostoses Syndrome 
Metaphyseal Anadysplasia +   
Meyenburg-Altherr-Uehlinger Syndrome 
Microcephaly Deafness Syndrome 
Microcephaly Seizures Genital Hypoplasia 
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies 
Muckle-Wells syndrome  
Multicystic Dysplastic Kidney +   
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Multiple Pterygium Syndrome, X-Linked 
multiple synostoses syndrome 1  
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
Myotubular Myopathy with Abnormal Genital Development 
Nathalie Syndrome 
Nephrosialidosis 
Nephrosis with Deafness and Urinary Tract and Digital Malformations 
nephrotic syndrome +   
Neu-Laxova syndrome 1  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES  
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME  
Nievergelt Syndrome 
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic deafness +   
Omphalocele Exstrophy Imperforate Anus 
Opticocochleodentate Degeneration 
Palant Cleft Palate Syndrome 
Penttinen-Aula Syndrome  
Perrault syndrome +   
Peters plus syndrome  
Piepkorn Karp Hickok syndrome 
Pointer Syndrome 
polydactyly +   
popliteal pterygium syndrome +   
postaxial acrofacial dysostosis  
Powell Chandra Saal Syndrome 
Proteus syndrome +   
Pulmonic Stenosis and Congenital Nephrosis 
Puromycin Aminonucleoside Nephrosis  
Pyelectasis 
Radial Ray Deficiency, X-Linked 
Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies  
Ramos Arroyo Clark Syndrome 
rapadilino syndrome  
Reardon Hall Slaney syndrome 
renal agenesis +   
Renal Dysplasia - Limb Defects Syndrome 
Renal, Genital, and Middle Ear Anomalies 
Retrocaval Ureter 
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Robinow syndrome +   
Rosselli-Gulienetti Syndrome 
Ruzicka Goerz Anton syndrome 
Schimke X-Linked Mental Retardation Syndrome 
Schlegelberger Grote Syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
Short Stature and Microcephaly with Genital Anomalies  
Short Stature-Obesity Syndrome 
Siddiqi syndrome  
Sinoatrial Node Dysfunction and Deafness  
spastic paraplegia with deafness 
Splenogonadal Fusion with Limb Defects and Micrognathia 
split hand-foot malformation +   
Split-Foot Malformation with Mesoaxial Polydactyly  
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects 
Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies 
Steinfeld Syndrome 
Stern Lubinsky Durrie Syndrome 
Stratton-Parker Syndrome 
Structural Heart Defects and Renal Anomalies Syndrome  
syndactyly +   
syndactyly-telecanthus-anogenital and renal malformations syndrome  
syndromic microphthalmia 6  
temtamy preaxial brachydactyly syndrome  
Tetramelic Monodactyly 
Tetramelic Postaxial Oligodactyly 
thanatophoric dysplasia +   
Thoracic Dysplasia-Hydrocephalus Syndrome 
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
Tietz syndrome  
Ulnar Hypoplasia with Mental Retardation 
Urinary Fistula +  
Urinary Tract Abnormalities +   
Uterine Anomalies 
VACTERL association +   
Viljoen Kallis Voges Syndrome 
Weill-Marchesani Syndrome 3  
Weyers acrofacial dysostosis  
Wright Dyck Syndrome 
X-linked Alport syndrome  
X-linked lissencephaly 2  
X-linked mental retardation Gustavson type  
X-linked mental retardation-hypotonic facies syndrome-1  
X-linked retinitis pigmentosa and sinorespiratory infections  
Yemenite Deaf-Blind Hypopigmentation Syndrome 
Yunis-Varon syndrome  

Synonyms
Exact Synonyms: Nephrosis Deafness Urinary Tract Digital Malformation
Primary IDs: MESH:C536402
Alternate IDs: MIM:256200

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