Disease #01162 (SPGF6 (spermatogenic failure, type 6 (SPGF-6, globozoospermia)), OMIM:102530)

Official abbreviation SPGF6
Name spermatogenic failure, type 6 (SPGF-6, globozoospermia)
OMIM ID 102530
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes GOPC, SPATA16
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

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00117913 - - male infertility M - China Han Chinese - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - SPGF6 non-obstructive azoospermia TEX11 TEX11 1 1 Fei Wang
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