Online Mendelian Inheritance in Man

Last uploaded: January 16, 2025

Id	http://purl.bioontology.org/ontology/OMIM/618086 http://purl.bioontology.org/ontology/OMIM/618086
Preferred Name	SPERMATOGENIC FAILURE 28
Synonyms	SPGF28
Type	http://www.w3.org/2002/07/owl#Class

altLabel	SPGF28
prefLabel	SPERMATOGENIC FAILURE 28
Gene Symbol	KIAA1596 SPGF28 POF15 FANCM
notation	618086
Scope Statement	Caused by mutation in the FANCM gene (FANCM, 609644.0003) [MOLECULAR BASIS]
OMIM MimType Value	pound
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000016
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
OMIM Entry Type	3
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU005254 http://purl.bioontology.org/ontology/OMIM/MTHU050419 http://purl.bioontology.org/ontology/OMIM/MTHU070549 http://purl.bioontology.org/ontology/OMIM/MTHU055533 http://purl.bioontology.org/ontology/OMIM/MTHU050418 http://purl.bioontology.org/ontology/OMIM/MTHU062305 http://purl.bioontology.org/ontology/OMIM/MTHU007248 See more See less
MIMTYPEMEANING	Phenotype description, molecular basis known.
Gene Locus	14q21.3
tui	T047
cui	C4748117

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