Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库

Last uploaded: September 7, 2023

Preferred Name	SPERMATOGENIC FAILURE 33
Synonyms	SPGF33
ID	http://purl.bioontology.org/ontology/OMIM/618152
altLabel	SPGF33
cui	C4748395
Gene Locus	12q24.31
Gene Symbol	SPGF33 CFAP251 WDR66
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU062595 http://purl.bioontology.org/ontology/OMIM/MTHU062591 http://purl.bioontology.org/ontology/OMIM/MTHU062593 http://purl.bioontology.org/ontology/OMIM/MTHU006969 http://purl.bioontology.org/ontology/OMIM/MTHU059322 http://purl.bioontology.org/ontology/OMIM/MTHU059324 http://purl.bioontology.org/ontology/OMIM/MTHU062248 http://purl.bioontology.org/ontology/OMIM/MTHU062594 http://purl.bioontology.org/ontology/OMIM/MTHU062592 http://purl.bioontology.org/ontology/OMIM/MTHU062596 http://purl.bioontology.org/ontology/OMIM/MTHU059325 http://purl.bioontology.org/ontology/OMIM/MTHU059321
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	618152
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	SPERMATOGENIC FAILURE 33
Scope Statement	Caused by mutation in the WD repeat-containing protein-66 gene (WDR66, 618146.0001) [MOLECULAR BASIS]
tui	T047

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://purl.obolibrary.org/obo/MONDO_0029147	Mondo Disease Ontology / Mondo疾病本体	LOOM
	http://purl.obolibrary.org/obo/DOID_0111915	Human Disease Ontology / 人类疾病本体	LOOM