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Term:
Noninsulin-Dependent Diabetes Mellitus with Deafness (DOID:9007177)
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Parent Terms Term With Siblings Child Terms
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency  
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
Absence of Tibia with Congenital Deafness 
Albinism Deafness Syndrome 
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
Ataxia and Polyneuropathy, Adult-Onset  
Ataxia Neuropathy Spectrum  
autosomal dominant keratitis-ichthyosis-deafness syndrome  
autosomal dominant nonsyndromic deafness 65  
Ayazi Syndrome 
Bjornstad syndrome  
Branchiogenic-Deafness Syndrome 
Burn-Mckeown Syndrome  
carbamoyl phosphate synthetase I deficiency disease  
Cardioauditory Syndrome of Sanchez Cascos 
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
Childhood Myocerebrohepatopathy Spectrum 
coenzyme Q10 deficiency disease +   
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
combined oxidative phosphorylation deficiency +   
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, and Onychodystrophy, Autosomal Dominant  
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
Congenital Myopathy with Neuropathy and Deafness  
Cowden-Like Syndrome  
Coxoauricular Syndrome 
cytochrome-c oxidase deficiency disease +   
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, Retinitis Pigmentosa, And Sperm Abnormalities 
Deafness, Congenital Onychodystrophy, Recessive Form 
Deafness, with Smith-Magenis Syndrome  
Deafness, X-Linked 6  
deafness-dystonia-optic neuronopathy syndrome  
Deoxyguanosine Kinase Deficiency  
Diabetes Mellitus, Noninsulin-Dependent, 1  
Diabetes Mellitus, Noninsulin-Dependent, 2 
Diabetes Mellitus, Noninsulin-Dependent, 3 
DIABETES MELLITUS, NONINSULIN-DEPENDENT, 5  
Diabetes Mellitus, Noninsulin-Dependent, Type 4 
diabetic ketoacidosis  
diabetic peripheral angiopathy 
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
early infantile epileptic encephalopathy 39  
ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2  
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
ethylmalonic encephalopathy  
Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young  
Fine-Lubinsky Syndrome 
Fountain Syndrome 
Friedreich ataxia +   
GRACILE syndrome  
hereditary spastic paraplegia 24 
Herrmann Syndrome 
high myopia-sensorineural deafness syndrome  
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hyperlipoproteinemia Type II, and Deafness 
Hypermetabolism due to Defect in Mitochondria 
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
hypomyelinating leukodystrophy 4  
hypotonia-cystinuria syndrome  
Ichthyosiform Erythroderma, Corneal Involvement, Deafness  
ITM2B-related cerebral amyloid angiopathy 2  
Johnson Neuroectodermal Syndrome 
Jones Syndrome 
Keipert Syndrome  
Konigsmark Knox Hussels Syndrome 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Leber hereditary optic neuropathy +   
Leigh disease +   
Lethal Encephalopathy due to Defective Mitochondrial and Peroxisomal Fission 1  
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation  
lipoatrophic diabetes mellitus +   
Lynch Lee Murday syndrome 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
maturity-onset diabetes of the young +   
Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency 
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1  
Meyenburg-Altherr-Uehlinger Syndrome 
Microcephaly Deafness Syndrome 
Mitochondrial Cardiomyopathy  
mitochondrial complex I deficiency +   
mitochondrial complex II deficiency  
mitochondrial complex III deficiency +   
mitochondrial complex V (ATP synthase) deficiency +   
Mitochondrial Cytopathy +   
mitochondrial DNA depletion syndrome +   
Mitochondrial Phosphate Carrier Deficiency  
mitochondrial pyruvate carrier deficiency  
Muckle-Wells syndrome  
multiple acyl-CoA dehydrogenase deficiency +   
multiple mitochondrial dysfunctions syndrome +   
Multiple Synostoses Syndrome 1  
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
Myopathy with Giant Abnormal Mitochondria 
Myopathy, Cataract, Hypogonadism Syndrome 
Nathalie Syndrome 
Nephrosis Deafness Urinary Tract Digital Malformation 
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic deafness +   
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
optic atrophy 1  
Opticocochleodentate Degeneration 
Parkinson's Disease, Mitochondrial  
Pearson syndrome  
Perrault syndrome +   
Progressive External Ophthalmoplegia with Hypogonadism 
Proximal Myopathy with Focal Depletion of Mitochondria 
pyruvate carboxylase deficiency disease +   
pyruvate decarboxylase deficiency +   
Ramos Arroyo Clark Syndrome 
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Sarcosinemia  
Schimke X-Linked Mental Retardation Syndrome 
Schlegelberger Grote Syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis  
SIDDIQI SYNDROME  
Sinoatrial Node Dysfunction and Deafness  
Spinocerebellar Ataxia with Epilepsy  
Succinate-Coa Ligase Deficiency +   
temtamy preaxial brachydactyly syndrome  
Tietz syndrome  
VDAC Deficiency 
very long chain acyl-CoA dehydrogenase deficiency  
Wells Jankovic Syndrome 
Wolfram syndrome 2  
Wright Dyck Syndrome 
X-linked Alport syndrome  
X-Linked Mental Retardation Gustavson Type 
X-Linked Retinitis Pigmentosa, and Sinorespiratory Infections, with or without Deafness  
Y-Linked Deafness +   
Yemenite Deaf-Blind Hypopigmentation Syndrome 

Synonyms
Exact Synonyms: Ballinger-Wallace Syndrome ;   Diabetes Mellitus, Type II, With Deafness ;   Diabetes mellitus, type 2, with deafness ;   Maternally Transmitted Diabetes-Deafness Syndrome ;   Maternally inherited diabetes and deafness ;   Mitochondrial Inherited Diabetes and Deafness ;   NIDDM with deafness
Primary IDs: MESH:C536246 ;   RDO:0001746

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.