Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/617187 http://purl.bioontology.org/ontology/OMIM/617187
Preferred Name	SPERMATOGENIC FAILURE 16
Synonyms	ACEPHALIC SPERMATOZOA SYNDROME SPGF16
Type	http://www.w3.org/2002/07/owl#Class

altLabel	ACEPHALIC SPERMATOZOA SYNDROME SPGF16
prefLabel	SPERMATOGENIC FAILURE 16
Gene Symbol	SUN5 SPGF16 SPAG4L TSARG4
Scope Statement	Caused by mutation in the SAD1 and UNC84 domain-containing protein-5 gene (SUN5, 613942.0001) [MOLECULAR BASIS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU056413 http://purl.bioontology.org/ontology/OMIM/MTHU040914 http://purl.bioontology.org/ontology/OMIM/MTHU006969 http://purl.bioontology.org/ontology/OMIM/MTHU056412 http://purl.bioontology.org/ontology/OMIM/MTHU056414 http://purl.bioontology.org/ontology/OMIM/MTHU018028 http://purl.bioontology.org/ontology/OMIM/MTHU056411 See more See less
tui	T047
Gene Locus	20q11.2
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	617187
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000016
cui	C4310674
OMIM Entry Type	3
OMIM MimType Value	pound

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