Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/618115 http://purl.bioontology.org/ontology/OMIM/618115
Preferred Name	SPERMATOGENIC FAILURE 32
Synonyms	SPGF32
Type	http://www.w3.org/2002/07/owl#Class

altLabel	SPGF32
prefLabel	SPERMATOGENIC FAILURE 32
Gene Symbol	TEB2 NOHLH SOHLH1 ODG5 SPGF32
Scope Statement	Caused by mutation in the spermatogenesis- and oogenesis-specific basic helix-loop-helix protein-1 gene (SOHLH1, 610224.0003) [MOLECULAR BASIS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU062438 http://purl.bioontology.org/ontology/OMIM/MTHU006969 http://purl.bioontology.org/ontology/OMIM/MTHU062439 http://purl.bioontology.org/ontology/OMIM/MTHU062440
tui	T047
Gene Locus	9q34.3
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	618115
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018
cui	C4748253
OMIM Entry Type	3
OMIM MimType Value	pound

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