Preferred Label : Spermatogenic failure, y-linked, 2;
Symbol : SPGFY2;
CISMeF acronym : SPGFY2;
Type : Phenotype, molecular basis known;
Alternative titles and symbols : Spermatogenic arrest, y-linked; Oligozoospermia, nonobstructive, y-linked; Oligospermia, nonobstructive, y-linked; Azoospermia, nonobstructive, y-linked; Spermatogenic failure, nonobstructive, y-linked;
Included titles and symbols : Azoospermia factor regions; Azf regions;
Description : About 2 to 3% of human males are infertile because of defects in sperm function, primarily
due to oligozoospermia (defined as less than 10-15 million sperm per mL of semen)
or azoospermia (Hull et al., 1985). - Heterogeneity of Spermatogenic Failure For a
discussion of Y-linked spermatogenic failure due to Sertoli cell-only syndrome, see
400042. For a discussion of phenotypic and genetic heterogeneity of spermatogenic
failure, see SPGF1 (258150).;
Inheritance : Y-linked (Yq11.23);
Prefixed ID : #415000;
Origin ID : 415000;
UMLS CUI : C1839071;
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
DO Cross reference
Genes related to phenotype
HPO term(s)
ORDO concept(s)
Related ORDO disease(s)
Semantic type(s)
UMLS correspondences (same concept)