Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023

Preferred Name	Cerebrocostomandibular Syndrome
Synonyms	Rib Gap Defects with Micrognathia
ID	http://purl.bioontology.org/ontology/MESH/C562538
altLabel	Rib Gap Defects with Micrognathia Cerebrocostomandibular-Like Syndrome CCM Syndrome
cui	C0265342 C3501912
Has mapping qualifier	http://purl.bioontology.org/ontology/MESH/Q000002
HM	D008607 D008844 D012272/Q000002
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D012272 http://purl.bioontology.org/ontology/MESH/D008607 http://purl.bioontology.org/ontology/MESH/D008844
MDA	20121105
MeSH Frequency	11
MMR	20131024
notation	C562538
prefLabel	Cerebrocostomandibular Syndrome
SC	3
TERMUI	T824987 T824986 T800906 T810781
TH	OMIM (2013)
tui	T047

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/OMIM/182282	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI
http://purl.obolibrary.org/obo/DOID_0111248	Human Disease Ontology / 人类疾病本体	LOOM
http://www.orpha.net/ORDO/Orphanet_1393	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM
http://www.orpha.net/ORDO/Orphanet_1393	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0007301	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0007301	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.bioontology.org/ontology/OMIM/117650	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI
http://purl.bioontology.org/ontology/OMIM/117650	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	LOOM