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Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n8	http://purl.obolibrary.org/obo/doid#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Subject Item: n2:DOID_12580
rdf:type: owl:Class
rdfs:subClassOf: n2:DOID_225 _:vb50948481 n2:DOID_0060388
rdfs:label: Cri-Du-Chat syndrome
rdfs:comment: OMIM mapping confirmed by DO. [SN].
wdrs:describedby: n7:doid.owl
obo:id: DOID:12580
obo:hasDbXref: NCI:C34518 OMIM:123450 MESH:D003410 GARD:6213 UMLS_CUI:C0010314 SNOMEDCT_US_2021_09_01:70173007 ICD10CM:Q93.4 ICD9CM:758.31
obo:hasExactSynonym: chromosome 5p deletion syndrome Cri-du-chat syndrome 5p deletion syndrome chromosome 5 short arm deletion syndrome 5p partial monosomy syndrome
obo:hasOBONamespace: disease_ontology
obo:inSubset: n8:NCIthesaurus
n2:IAO_0000115: A syndrome that has_material_basis_in deletion of the end of the chromosome 5 p arm and that is characterized by intellectual disability, delayed development, small head size, low birth weight, weak muscle tone widely set eyes, low-set ears, a small jaw, a rounded face and a high-pitched cry that sounds like that of a cat.