Phenotypes for disease #03824 (SPGF11 (spermatogenic failure, type 11 (SPGF-11)), OMIM:615081)

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     

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Owner     

Individual ID     
0000296643 28y female with progressive spastic paraparesis, mental retardation, slurred speech and pes cavus HSP SPG11 Familial, autosomal recessive 28y - 16y - - Sherifa Ahmed Hamed 00404050
0000296687 28-y male with delayed mental development. He developed progressive spastic lower limbs, wasting of small muscles of the hands and pes cavus. He has two paternal male uncles with similar condition. HSP SPG11 Familial, autosomal recessive 28y - 12y - - Sherifa Ahmed Hamed 00404098
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