Disease #06958 (SPGFX4 (spermatogenic failure, X-linked, type 4), OMIM:301077)

Official abbreviation SPGFX4
Name spermatogenic failure, X-linked, type 4
OMIM ID 301077
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ACRC
Associated tissues -
Disease features -
Remarks -
Date created 2022-08-19 17:17:03 +02:00 (CEST)
Date last edited N/A

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