Spermatogenic failure 3

Preferred Label : Spermatogenic failure 3;

Symbol : SPGF3;

CISMeF acronym : SPGF3;

Type : Phenotype, molecular basis known;

Description : For a discussion of phenotypic and genetic heterogeneity of spermatogenic failure, see SPGF1 (258150).;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the solute carrier family 26 (sulfate transporter), member 8 gene (SLC26A8, 608480.0001);

Prefixed ID : #606766;

Details

Origin ID

606766;

UMLS CUI

C4721889;

Automatic exact mappings (from CISMeF team)
- azoospermia, nonobstructive [MeSH concept]
- azoospermia, nonobstructive [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- spermatogenic failure 3 [DO Concept]
DO Cross reference
- spermatogenic failure 3 [DO Concept]
Genes related to phenotype
- Solute carrier family 26 (sulfate transporter), member 8 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Infertility [HPO term]
ORDO concept(s)
- Non-syndromic male infertility due to sperm motility disorder [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- azoospermia, nonobstructive [MeSH Supplementary Concept]
- azoospermia, nonobstructive [MeSH concept]
- spermatogenic failure 3 [DO Concept]

Keyword's position in hierarchy(ies) :

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