Disease #06931 (SPGF48 (spermatogenic failure, type 48), OMIM:619108)

Official abbreviation SPGF48
Name spermatogenic failure, type 48
OMIM ID 619108
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 M1AP
Associated tissues -
Disease features -
Remarks -