Phenotypes for disease #06849 (MRXS99F (Mental retardation, X-linked 99, syndromic, female-restricted), OMIM:300968)

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

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000325274 - - Gait disturbance, Pes cavus, Scoliosis, Abnormality of eye movement, Brain imaging abnormality, Scheuermann-like vertebral changes Unknown 22y - - - Andreas Laner 00435031
0000357086 - - Seizure, eyelid myoclonus and activity arrest from the age of 2 Isolated (sporadic) 03y - - - Andreas Laner 00472278
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