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Ontology Browser

Term:
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease (DOID:9004315)
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Parent Terms Term With Siblings Child Terms
46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs  
Acrootoocular Syndrome 
AIDS-Associated Nephropathy  
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 
Alexander Disease  
Alsing Syndrome 
aminoglycoside-induced deafness  
anuria +   
aortic atherosclerosis  
Arnold Stickler Bourne Syndrome 
Ataxia, Deafness, and Cardiomyopathy 
Athabaskan brainstem dysgenesis syndrome  
atheroembolism of kidney 
Auditory Neuropathy, Nonsyndromic Recessive 
Autoimmune Interstitial Lung, Joint, and Kidney Disease  
autosomal dominant cerebellar ataxia, deafness and narcolepsy  
autosomal dominant nonsyndromic deafness +   
autosomal recessive nonsyndromic deafness +   
autosomal recessive spinocerebellar ataxia 19  
autosomal-mitochondrial sensorineural deafness  
Axenfeld-Rieger Anomaly with Cardiac Defects and Sensorineural Hearing Loss 
Ayme-Gripp syndrome  
BADS syndrome 
Bart-Pumphrey syndrome  
Bartter disease type 4A  
Bartter disease type 4b  
Bifid Nose with or without Anorectal And Renal Anomalies  
Bjornstad syndrome  
Blue Diaper Syndrome 
Boudhina Yedes Khiari syndrome 
Brachydactyly, Intraventricular Septal Defect, and Deafness 
Brown-Vialetto-Van Laere syndrome +   
CAKUT1  
Canavan disease  
CAPOS Syndrome  
Carotid Atherosclerosis  
Carotid Intimal Medial Thickness 1  
Cataract Ataxia Deafness 
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA  
Cerebellar Ataxia and Hypergonadotropic Hypogonadism 
Cerebellar Ataxia and Neurosensory Deafness 
cerebral atherosclerosis 
Cerebrocortical Degeneration of Infancy 
Charcot-Marie-Tooth disease type 1E  
Charcot-Marie-Tooth disease type 2J  
Charcot-Marie-Tooth disease X-linked recessive 4  
childhood spinal muscular atrophy +   
Chitty Hall Baraitser Syndrome 
Chudley-Mccullough syndrome  
Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss 
Cochleosaccular Degeneration of the Inner Ear and Progressive Cataracts 
Cockayne syndrome +   
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus  
Combined Pituitary Hormone Deficiency, 3  
Complement Factor H Deficiency  
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Congenital Deafness with Total Albinism 
Congenital Ectodermal Dysplasia with Hearing Loss 
Congenital Muscular Dystrophy with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers 
corneal dystrophy-perceptive deafness syndrome  
cortical deafness +   
craniofacial-deafness-hand syndrome  
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness  
cystic kidney disease +   
De Hauwere syndrome 
Deafness Oligodontia Syndrome 
Deafness, High-Frequency Sensorineural, X-Linked 
Deafness, Progressive High-Tone Neural 
deafness-intellectual disability, Martin-Probst type syndrome  
Diabetes Complications +   
diabetes insipidus +   
Diabetes Mellitus, Congenital Autoimmune  
Diabetes Mellitus, Experimental   
Diabetes Mellitus, New-Onset after Transplantation  
Diabetic Nephropathies  
dilated cardiomyopathy 1J  
Dimauro Disease  
dioctophymiasis 
distal arthrogryposis type 6 
Distal Renal Tubular Acidosis with Progressive Nerve Deafness  
Distal Renal Tubular Acidosis, Autosomal Recessive, with Late-Onset Sensorineural Hearing Loss  
dominant optic atrophy plus syndrome  
Donnai-Barrow syndrome  
Donohue syndrome  
DOORS syndrome  
Dystonia Musculorum Deformans +   
EAST syndrome  
Ectodermal Dysplasia and Neurosensory Deafness 
Ectodermal Dysplasia, Sensorineural Hearing Loss, and Distinctive Facial Features 
Ermine Phenotype 
Familial Amyloid Polyneuropathies +   
familial encephalopathy with neuroserpin inclusion bodies  
familial juvenile hyperuricemic nephropathy +   
Feigenbaum Bergeron Richardson Syndrome 
Fitzsimmons Walson Mellor Syndrome 
Flynn Aird Syndrome 
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness 
Furukawa Takagi Nakao Syndrome 
Gemignani Syndrome 
generalized atherosclerosis 
Generalized Lipodystrophy with Mental Retardation, Deafness, Short Stature, and Slender Bones 
Gerstmann-Straussler-Scheinker syndrome  
gestational diabetes +   
Gilles de la Tourette syndrome +   
Glomerular Diseases +   
Gonadal Dysgenesis, XX Type, with Deafness +   
Goodpasture syndrome +   
granulomatosis with polyangiitis +   
Griscelli syndrome +   
Hantavirus hemorrhagic fever with renal syndrome +   
Hearing Loss, Cisplatin-Induced  
Hearing Loss, Noise-Induced  
Hearing Loss, Unilateral Sensorineural  
Heimler syndrome 1  
Hereditary Central Nervous System Demyelinating Diseases +   
Hereditary Optic Atrophies +   
hereditary sensory neuropathy +   
Herrmann Syndrome 
HID Syndrome  
high myopia-sensorineural deafness syndrome  
High-Frequency Hearing Loss  
histiocytosis-lymphadenopathy plus syndrome  
Hittner Hirsch Kreh Syndrome  
Homozygous 11p15-p14 Deletion Syndrome 
Huntington's disease +   
Huntington's disease-like 2  
Huntington's Disease-Like Syndrome  
Hydranencephaly with Renal Aplasia-Dysplasia  
hydronephrosis +   
Hyperoxaluria +   
Hyperproinsulinemia  
hypoparathyroidism-deafness-renal disease syndrome  
hypophosphatemic nephrolithiasis/osteoporosis +   
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
Infundibulopelvic Dysgenesis 
Insulin-Like Growth Factor I Deficiency  
Insulin-Resistant Diabetes Mellitus, with Acanthosis Nigricans  
Jejunal Atresia with Renal Adysplasia 
Johanson-Blizzard syndrome  
Joubert syndrome 5  
Joubert syndrome 6  
Joubert syndrome 9  
Kennedy's disease  
kidney cortex disease +  
kidney failure +   
kidney hypertrophy 
Kidney Neoplasms +   
kidney papillary necrosis 
Lachiewicz Sibley Syndrome 
Lafora disease  
Latent Autoimmune Diabetes in Adults  
Leukoencephalomyelopathy  
Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules 
Lipodystrophy with Congenital Cataracts and Neurodegeneration  
Lipoprotein Glomerulopathy  
Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus  
Marshall syndrome +   
Martinez-Frias Syndrome 
Mental Retardation, X-Linked +   
Microcephaly, Epilepsy, and Diabetes Syndrome  
Mid-Tone Neural Deafness 
Mitchell-Riley Syndrome  
mitochondrial DNA depletion syndrome 6  
Mitochondrial Myopathy with Diabetes 
motor peripheral neuropathy +   
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
MYH-9 related disease +   
myotonia congenita +   
myotonic dystrophy type 1 +   
neonatal diabetes mellitus +   
nephritis +   
nephrocalcinosis +   
nephrogenic diabetes insipidus +   
nephrolithiasis +   
nephronophthisis-like nephropathy 1  
Nephropathy Deafness Hyperparathyroidism 
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness  
nephrosclerosis +   
neuroacanthocytosis +   
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES  
Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia 
neurofibromatosis +   
neurogenic scapuloperoneal syndrome Kaeser type  
neuronal ceroid lipofuscinosis +   
Nonsyndromic Sensorineural Hearing Loss +   
obstructive nephropathy  
ocular albinism with sensorineural deafness  
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Opticocochleodentate Degeneration 
orthostatic proteinuria 
Otodental Dysplasia 
Otofacioosseous-Gonadal Syndrome 
otospondylomegaepiphyseal dysplasia  
palmoplantar keratoderma-deafness syndrome  
pancreatic hypoplasia-diabetes-congenital heart disease syndrome  
pantothenate kinase-associated neurodegeneration +   
Paragangliomas with Sensorineural Hearing Loss  
PCWH syndrome  
Pendred syndrome  
perinephritis 
peripheral artery disease +   
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
Pfeiffer Kapferer Syndrome 
Pigmentary Retinopathy and Sensorineural Deafness  
PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES  
prediabetes syndrome  
Premature Aging, Okamoto Type 
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
Presbycusis +   
primary cerebellar degeneration +   
Progressive Nephropathy with Deafness 
Progressive Psychomotor Deterioration  
proteinuria +   
Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness 
pyelitis +   
Radiation Nephropathy  
Radio Renal Syndrome 
renal agenesis +   
renal artery atheroma 
renal artery disease +   
renal artery obstruction +   
Renal Dysplasia - Limb Defects Syndrome 
renal fibrosis +   
renal hypertension +   
renal hypoplasia +   
renal infectious disease 
Renal Ischemia  
Renal Nutcracker Syndrome 
renal osteodystrophy  
renal tuberculosis  
Renal Tubular Dysgenesis  
renal tubular transport disease +   
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA 
Retinitis Pigmentosa Inversa with Deafness 
Robinson Miller Bensimon Syndrome 
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction 
Schaap Taylor Baraitser Syndrome 
secondary hyperparathyroidism of renal origin 
Selig Benacerraf Greene Syndrome 
Sensorineural Deafness and Male Infertility  
Sensorineural Deafness and Migraine  
Sensorineural Deafness with Hypertrophic Cardiomyopathy  
Sensorineural Deafness with Mild Renal Dysfunction  
Sensorineural Deafness with Peripheral Neuropathy and Arterial Disease 
Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth 
Siegler Brewer Carey Syndrome 
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 
spinal muscular atrophy with lower extremity predominance +   
split hand-foot malformation 1 with sensorineural hearing loss  
Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness 
Spongiform Encephalopathy with Neuropsychiatric Features  
stricture or kinking of ureter 
Sudden Hearing Loss  
syndromic microphthalmia 10 
thiamine-responsive megaloblastic anemia syndrome  
Thrombocytopenia with Elevated Serum Iga and Renal Disease 
Thyrocerebral-Retinal Syndrome 
Townes-Brocks syndrome +   
Treft Sanborn Carey Syndrome 
tuberous sclerosis +   
Tunglang Savage Bellman Syndrome 
type 1 diabetes mellitus +   
type 2 diabetes mellitus +   
Unverricht-Lundborg syndrome +   
uremia +   
Usher syndrome +   
uveal coloboma-cleft lip and palate-intellectual disability  
Vohwinkel syndrome  
WEBB-DATTANI SYNDROME  
Wilson disease +   
Wolfram syndrome 2  
Wolfram syndrome, mitochondrial form 
Woodhouse-Sakati Syndrome  
X-linked nonsyndromic deafness +   
Yorifuji Okuno Syndrome 
Zellweger syndrome +   

Synonyms
Primary IDs: MESH:C565928
Alternate IDs: RDO:0014435

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