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Metadata
ID DOID:0112176
Name spermatogenic failure 48
Definition A spermatogenic failure that is characterized by impaired spermatogenesis, primarily occurring at meiosis that has_material_basis_in homozygous or compound heterozygous mutation in M1AP on chromosome 2p13.1.
https://pubmed.ncbi.nlm.nih.gov/32017041/, https://pubmed.ncbi.nlm.nih.gov/32673564/
Xrefs

OMIM:619108

Synonyms

SPGF48 [EXACT]

Parent Relationships

is_a spermatogenic failure

is_a autosomal recessive disease

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