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Ontology Browser

Term:
Cerebellar Ataxia and Hypergonadotropic Hypogonadism (DOID:9001089)
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Parent Terms Term With Siblings Child Terms
cerebellar ataxia +     
hypogonadism +     
3-methylglutaconic aciduria type 5  
Acrootoocular Syndrome 
Alopecia, Hypogonadism, Extrapyramidal Disorder 
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism 
Arthrogryposis-like Hand Anomaly and Sensorineural Deafness 
ataxia with oculomotor apraxia type 1  
Ataxia, Deafness, and Cardiomyopathy 
Athabaskan brainstem dysgenesis syndrome  
Auditory Neuropathy, Nonsyndromic Recessive 
autosomal dominant cerebellar ataxia +   
autosomal dominant cerebellar ataxia, deafness and narcolepsy  
autosomal dominant nonsyndromic deafness +   
autosomal recessive cerebellar ataxia +   
autosomal recessive nonsyndromic deafness +   
autosomal recessive spinocerebellar ataxia 19  
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  
Bassoe Syndrome 
Benign Cerebellar Ataxia with Thermoanalgesia 
Biemond Syndrome II 
Bjornstad syndrome  
Borjeson-Forssman-Lehmann syndrome  
Boucher-Neuhauser syndrome  
Boudhina Yedes Khiari syndrome 
Brachydactyly, Intraventricular Septal Defect, and Deafness 
Brachydactyly-Nystagmus-Cerebellar Ataxia 
Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia 
Brown-Vialetto-Van Laere syndrome +   
Cantalamessa Baldini Ambrosi Syndrome 
CAPOS Syndrome  
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cataract Ataxia Deafness 
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA  
Cayman type cerebellar ataxia  
Cerebellar Ataxia and Hypergonadotropic Hypogonadism 
Cerebellar Ataxia and Hypogonadotropic Hypogonadism  
Cerebellar Ataxia and Neurosensory Deafness 
Cerebellar Ataxia Ectodermal Dysplasia 
CEREBELLAR ATAXIA INFANTILE WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA  
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME  
Cerebellar Hypoplasia with Endosteal Sclerosis  
Cerebellofaciodental Syndrome  
Cerebelloparenchymal Disorder II 
Chang Davidson Carlson Syndrome 
Charcot-Marie-Tooth disease type 1E  
Charcot-Marie-Tooth disease type 2J  
Charcot-Marie-Tooth disease X-linked recessive 4  
Chitty Hall Baraitser Syndrome 
Chudley-Mccullough syndrome  
Chudley-Rozdilsky Syndrome 
Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss 
Cochleosaccular Degeneration of the Inner Ear and Progressive Cataracts 
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus  
Combined Pituitary Hormone Deficiency, 3  
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Congenital Deafness, with Total Albinism 
Congenital Ectodermal Dysplasia with Hearing Loss 
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism 
Corneal Dystrophy and Perceptive Deafness  
CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA  
cortical deafness +   
craniofacial-deafness-hand syndrome  
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness  
De Hauwere syndrome 
De Sanctis-Cacchione Syndrome  
Deafness Enamel Hypoplasia Nail Defects  
Deafness Oligodontia Syndrome 
Deafness, Aminoglycoside-Induced  
Deafness, High-Frequency Sensorineural, X-Linked  
Deafness, Mid-Tone Neural 
Deafness, Progressive High-Tone Neural 
Deafness, X-Linked 1  
Deafness, X-Linked 3 
Deafness, X-Linked 4  
Deafness, X-Linked 5  
Deafness-Hypogonadism Syndrome 
deafness-intellectual disability, Martin-Probst type syndrome  
Digitorenocerebral Syndrome  
dilated cardiomyopathy 1J  
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  
EAST syndrome  
Ectodermal Dysplasia and Neurosensory Deafness 
Ectodermal Dysplasia, Sensorineural Hearing Loss, and Distinctive Facial Features 
Encephalopathy, Spastic Tetraparesis, and Hypogonadism 
episodic ataxia type 5  
episodic ataxia type 6  
Ermine Phenotype 
eunuchism +   
familial hemiplegic migraine 1  
Fitzsimmons Walson Mellor Syndrome 
Flynn Aird Syndrome 
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness 
Furukawa Takagi Nakao Syndrome 
Gemignani Syndrome 
Generalized Lipodystrophy, with Mental Retardation, Deafness, Short Stature, and Slender Bones 
Gillespie Syndrome  
gonadal dysgenesis +   
Gonadal Dysgenesis, XX Type, with Deafness +   
Griscelli syndrome +   
Harding Ataxia 
Hearing Loss, Cisplatin-Induced  
Hearing Loss, Noise-Induced  
Hearing Loss, Unilateral Sensorineural  
Herrmann Syndrome 
HID Syndrome  
High-Frequency Hearing Loss  
histiocytosis-lymphadenopathy plus syndrome  
Hittner Hirsch Kreh Syndrome 
Homozygous 11p15-p14 Deletion Syndrome 
Hypergonadotropic Hypogonadism And Partial Alopecia 
Hypogonadism and Testicular Atrophy 
Hypogonadism with Low-Grade Mental Deficiency and Microcephaly 
hypogonadotropic hypogonadism +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
hypoparathyroidism-deafness-renal disease syndrome  
Ichthyosis and Male Hypogonadism 
Insulin-Like Growth Factor I Deficiency  
Isolated Mineralocorticoid Deficiency  
ITM2B-related cerebral amyloid angiopathy 2  
Johanson-Blizzard syndrome  
Johnson Neuroectodermal Syndrome 
Klinefelter's syndrome  
Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy 
Lubinsky Syndrome 
Male Hypogonadism with Mental Retardation and Skeletal Anomalies 
Malouf Syndrome  
Marinesco-Sjogren syndrome  
Marshall syndrome +   
Martsolf syndrome  
MEHMO syndrome  
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1  
Moebius Axonal Neuropathy Hypogonadism 
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism  
Myelocerebellar Disorder  
MYH-9 related disease +   
Myoclonus, Cerebellar Ataxia, and Deafness 
Myopathy, Cataract, Hypogonadism Syndrome 
Nephropathy Deafness Hyperparathyroidism 
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness  
Neuhauser Eichner Opitz Syndrome 
Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia 
nonprogressive cerebellar ataxia with mental retardation  
Nonsyndromic Sensorineural Hearing Loss  
ocular albinism with sensorineural deafness  
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Otodental Dysplasia 
Otofacioosseous-Gonadal Syndrome 
otospondylomegaepiphyseal dysplasia  
palmoplantar keratoderma-deafness syndrome  
Paragangliomas with Sensorineural Hearing Loss  
Pendred syndrome  
Pfeiffer Kapferer Syndrome 
Pigmentary Retinopathy and Sensorineural Deafness  
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
Presbycusis +   
Progressive External Ophthalmoplegia with Hypogonadism 
Progressive Hearing Loss Stapes Fixation  
Progressive Nephropathy with Deafness 
Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness 
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA 
Retinitis Pigmentosa Inversa with Deafness 
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 
Richards-Rundle Syndrome 
Robinson Miller Bensimon Syndrome 
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction 
Rud Syndrome 
Schaap Taylor Baraitser Syndrome 
Scholte Syndrome 
Seemanova Lesny 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 Deafness, Autosomal-Mitochondrial Type  
Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth 
Sexual Infantilism  
short-rib thoracic dysplasia 9 with or without polydactyly  
Slti Salem Syndrome 
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 
split hand-foot malformation 1 with sensorineural hearing loss  
Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness 
Sudden Hearing Loss  
syndromic X-linked intellectual disability Cabezas type  
thiamine-responsive megaloblastic anemia syndrome  
Townes-Brocks syndrome +   
Treft Sanborn Carey Syndrome 
Tunglang Savage Bellman Syndrome 
Usher syndrome +   
uveal coloboma-cleft lip and palate-intellectual disability  
Vasquez Hurst Sotos Syndrome 
Vohwinkel syndrome  
Warburg micro syndrome +   
Weinstein Kliman Scully Syndrome 
Wolfram syndrome 2  
Wolfram syndrome, mitochondrial form 
Woodhouse-Sakati Syndrome  
X-linked nonsyndromic deafness +   
Young Hughes Syndrome 

Synonyms
Primary IDs: MESH:C565308
Alternate IDs: RDO:0013982

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