Online Mendelian Inheritance in Man

Last uploaded: January 16, 2025

Id	http://purl.bioontology.org/ontology/OMIM/620897 http://purl.bioontology.org/ontology/OMIM/620897
Preferred Name	OVARIAN DYSGENESIS 11
Synonyms	ODG11
Type	http://www.w3.org/2002/07/owl#Class

altLabel	ODG11
prefLabel	OVARIAN DYSGENESIS 11
Gene Symbol	MCM8IP ODG11 HROB C17orf53
notation	620897
Scope Statement	Caused by mutation in the homologous recombination factor with OB-fold gene (HROB, 618611.0001) [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/MTHU061556 http://purl.bioontology.org/ontology/OMIM/MTHU078771 http://purl.bioontology.org/ontology/OMIM/MTHU077079 http://purl.bioontology.org/ontology/OMIM/MTHU050419 http://purl.bioontology.org/ontology/OMIM/MTHU050418 http://purl.bioontology.org/ontology/OMIM/MTHU036721 http://purl.bioontology.org/ontology/OMIM/MTHU037476 http://purl.bioontology.org/ontology/OMIM/MTHU078770 http://purl.bioontology.org/ontology/OMIM/MTHU036761 See more See less
MIMTYPEMEANING	Phenotype description, molecular basis known.
Gene Locus	17q21.31
tui	T047
cui	C5935637

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