Disease #03824 (SPGF11 (spermatogenic failure, type 11 (SPGF-11)), OMIM:615081)

Official abbreviation SPGF11
Name spermatogenic failure, type 11 (SPGF-11)
OMIM ID 615081
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene KLHL10
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00404050 - - - F - Egypt - - - - - SPGF11 28y female with progressive spastic paraparesis, mental retardation, slurred speech and pes cavus SPG11 SPG11 1 2 Sherifa Ahmed Hamed
00404098 - - - M yes Egypt - - - - - SPGF11 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. SPG11 SPG11 1 2 Sherifa Ahmed Hamed
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