Disease #06908 (SPGF50 (spermatogenic failure, type 50), OMIM:619145)

Official abbreviation SPGF50
Name spermatogenic failure, type 50
OMIM ID 619145
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene XRCC2
Associated tissues -
Disease features -
Remarks -