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Ontology Browser

Term:
Encephalopathy, Spastic Tetraparesis, and Hypogonadism (DOID:9008075)
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Parent Terms Term With Siblings Child Terms
hypogonadism +     
Muscle Spasticity +     
Paresis +     
2-hydroxyglutaric aciduria +   
adrenoleukodystrophy +   
Alopecia, Hypogonadism, Extrapyramidal Disorder  
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism 
Asparagine Synthetase Deficiency  
Bassoe Syndrome 
Biemond Syndrome II 
Borjeson-Forssman-Lehmann syndrome  
Boucher-Neuhauser syndrome  
branched-chain keto acid dehydrogenase kinase deficiency  
Cantalamessa Baldini Ambrosi Syndrome 
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cerebellar Ataxia and Hypergonadotropic Hypogonadism 
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
Chang Davidson Carlson Syndrome 
Childhood-Onset Spasticity with Hyperglycinemia  
Chudley-Rozdilsky Syndrome 
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism 
creatine transporter deficiency  
CST3-related cerebral amyloid angiopathy +   
De Sanctis-Cacchione Syndrome  
Deafness-Hypogonadism Syndrome 
Defect of Tricarboxylic Acid Cycle 
Diaminopentanuria 
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome  
dystonia 9  
encephalopathy due to defective mitochondrial and peroxisomal fission 1  
ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2  
Encephalopathy, Spastic Tetraparesis, and Hypogonadism 
eunuchism +   
Fitzsimmons Walson Mellor Syndrome 
galactosemia +   
glycine encephalopathy +   
gonadal dysgenesis +   
Hartnup disease  
Hereditary Central Nervous System Demyelinating Diseases +   
Hhhh Syndrome 
homocarnosinosis  
homocystinuria +   
hyperlysinemia +   
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  
Ichthyosis and Male Hypogonadism 
Isolated Mineralocorticoid Deficiency  
Johnson Neuroectodermal Syndrome 
Klinefelter syndrome  
Koone Rizzo Elias Syndrome 
Leigh disease +   
Lesch-Nyhan syndrome +   
Lubinsky Syndrome 
Lysosomal Storage Diseases, Nervous System +   
Male Hypogonadism with Mental Retardation and Skeletal Anomalies 
maple syrup urine disease +   
Martsolf syndrome  
MEHMO syndrome  
MELAS syndrome +   
Menkes disease +   
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1  
MERRF Syndrome +   
Methylenetetrahydrofolate Reductase Deficiency  
mevalonic aciduria  
Microphthalmia and Mental Deficiency 
Moebius Axonal Neuropathy Hypogonadism 
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism  
Myopathy, Cataract, Hypogonadism Syndrome 
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY  
Neurodevelopmental Disorder with Microcephaly, Cortical Malformations, and Spasticity  
NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH  
oculocerebrorenal syndrome +   
Opticocochleodentate Degeneration 
Paraparesis +   
phenylketonuria +   
Powell Venencie Gordon syndrome 
Progressive External Ophthalmoplegia with Hypogonadism 
pyruvate carboxylase deficiency disease +   
pyruvate decarboxylase deficiency +   
Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression  
Refsum disease +   
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 
Richards-Rundle Syndrome 
Rud Syndrome 
Scholte Syndrome 
Seemanova Lesny Syndrome 
Severe Mental Retardation, with Spasticity and Pigmentary Tapetoretinal Degeneration 
Sexual Infantilism  
Silengo Lerone Pelizza Syndrome 
Slti Salem Syndrome 
spastic ataxia +   
Spastic Ataxia with Congenital Miosis 
syndromic X-linked intellectual disability Cabezas type  
syndromic X-linked intellectual disability Turner type  
tyrosinemia +   
urea cycle disorder +   
Vasquez Hurst Sotos Syndrome 
Warburg micro syndrome +   
Webb-Dattani Syndrome  
Weinstein Kliman Scully Syndrome 
Wells Jankovic Syndrome 
Wilson disease +   
Woodhouse-Sakati Syndrome  
X-linked intellectual disability-psychosis-macroorchidism syndrome  
Young Hughes Syndrome 
Zellweger syndrome +   

Synonyms
Primary IDs: MESH:C565722 ;   RDO:0014281

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