Disease #06929 (SPGF51 (spermatogenic failure, type 51), OMIM:619177)

Official abbreviation SPGF51
Name spermatogenic failure, type 51
OMIM ID 619177
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 MAATS1
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 27
LOVD software ©2004-2022 Leiden University Medical Center 		There are currently no updates.