Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	CONGENITAL SHORT BOWEL SYNDROME
Synonyms	CSBS
ID	http://purl.bioontology.org/ontology/OMIM/615237
altLabel	CSBS
cui	C0021847
Gene Locus	11q24.1
Gene Symbol	CLMP ASAM ACAM CSBS
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU049493 http://purl.bioontology.org/ontology/OMIM/MTHU009718 http://purl.bioontology.org/ontology/OMIM/MTHU000081 http://purl.bioontology.org/ontology/OMIM/MTHU050890 http://purl.bioontology.org/ontology/OMIM/MTHU050886 http://purl.bioontology.org/ontology/OMIM/MTHU004140 http://purl.bioontology.org/ontology/OMIM/MTHU050888 http://purl.bioontology.org/ontology/OMIM/MTHU050889 http://purl.bioontology.org/ontology/OMIM/MTHU050887 http://purl.bioontology.org/ontology/OMIM/MTHU005778 http://purl.bioontology.org/ontology/OMIM/MTHU050891 http://purl.bioontology.org/ontology/OMIM/MTHU050885
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	615237
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	CONGENITAL SHORT BOWEL SYNDROME
tui	T047

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/D007418	Medical Subject Headings	CUI