Phenotypes for disease #03634 (SPG46 (paraplegia, spastic, type 46, autosomal recessive (SPG-46)), OMIM:614409)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000041536 hereditary spastic paraplegia, ataxia, cataract, neuropathy, mild ID, thin corpus callosum, white matter changes hereditary spastic paraplegia SPG46 Familial, autosomal recessive - - 03y - - Erik-Jan Kamsteeg 00054872
0000226759 Dementia Ataxia Dystonia Dementia SPG-46 Familial, autosomal recessive - - - - - Katja Kloth 00299449
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