Phenotypes for disease #03777 (PBD12A (peroxisome biogenesis disorder, type 12A (PBD12A)), OMIM:614886)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000257416 Sibling pair, both with a history of developmental delay presenting at 7 and 8 years of age with progressive ataxia, occasional myoclonus and TCS and dementia. Associated with limb spasticity. progressive myoclonus epilepsy , dementia - Familial, autosomal recessive - - - - - Johan den Dunnen 00334927
0000257417 see sib progressive myoclonus epilepsy , dementia - Familial, autosomal recessive - - - - - Johan den Dunnen 00334928
0000257424 Onset age 8 ataxia, then TCS from age 12, on a background of normal developmental history prior to onset. Progressive severe ataxia. Hypertonia noted. Death age 35. (Affected brother not recruited) progressive myoclonus epilepsy , dementia - Familial, autosomal recessive - - - - - Johan den Dunnen 00334930
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