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Metadata
ID DOID:0070577
Name spermatogenic failure 78
Definition A spermatogenic failure characterized by sperm with abnormal acrosome structure due to a manchette assembly defect that has_material_basis_in homozygous mutation in the IQCN gene on chromosome 19p13.11.
https://pubmed.ncbi.nlm.nih.gov/36321563/
Xrefs

MIM:620170

SKOS

exactMatch MIM:620170

Synonyms

SPGF78 [EXACT]

Parent Relationships

is_a spermatogenic failure

is_a autosomal recessive disease

Subclass Logical Relationships

has material basis in some autosomal recessive inheritance

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