Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/614326 http://purl.bioontology.org/ontology/OMIM/614326
Preferred Name	FEINGOLD SYNDROME 2
Synonyms	FGLDS2 BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY
Type	http://www.w3.org/2002/07/owl#Class

altLabel	FGLDS2 BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY
prefLabel	FEINGOLD SYNDROME 2
Gene Symbol	FGLDS2
Scope Statement	Contiguous gene syndrome caused by deletion of 180 kb on 13q31.3 encompassing the micro RNA 17 host gene (MIR17HG, 609415) [MOLECULAR BASIS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU036340 http://purl.bioontology.org/ontology/OMIM/MTHU009585 http://purl.bioontology.org/ontology/OMIM/MTHU003197 http://purl.bioontology.org/ontology/OMIM/MTHU004733 http://purl.bioontology.org/ontology/OMIM/MTHU061712 http://purl.bioontology.org/ontology/OMIM/MTHU009211 http://purl.bioontology.org/ontology/OMIM/MTHU015647 http://purl.bioontology.org/ontology/OMIM/MTHU004024 http://purl.bioontology.org/ontology/OMIM/MTHU072600 http://purl.bioontology.org/ontology/OMIM/MTHU004822 http://purl.bioontology.org/ontology/OMIM/MTHU000145 http://purl.bioontology.org/ontology/OMIM/MTHU035640 http://purl.bioontology.org/ontology/OMIM/MTHU072599 See more See less
tui	T047
Gene Locus	13q31.3
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	614326
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018
cui	C3280489
OMIM Entry Type	3
OMIM MimType Value	pound

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