Medical Subject Headings

Last uploaded: November 5, 2019

Preferred Name	Robinow Syndrome, Autosomal Dominant
Synonyms	Robinow Syndrome
ID	http://purl.bioontology.org/ontology/MESH/C562492
altLabel	Robinow Syndrome Fetal Face Syndrome Robinow-Silverman-Smith Syndrome Robinow Dwarfism Acral Dysostosis with Facial and Genital Abnormalities Mesomelic Dwarfism-Small Genitalia Syndrome
cui	C0265205 C4551476
HM	D019465 D014564 D004392 D017880
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D017880 http://purl.bioontology.org/ontology/MESH/D019465 http://purl.bioontology.org/ontology/MESH/D014564 http://purl.bioontology.org/ontology/MESH/D004392
MDA	20121105
MeSH Frequency	12
MMR	20131024
notation	C562492
prefLabel	Robinow Syndrome, Autosomal Dominant
SC	3
TERMUI	T800805 T842405 T826479 T800806 T842406 T842404 T800803
TH	OMIM (2013) GHR (2014)
tui	T047

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/OMIM/164975	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/ICD10CM/Q87.1	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/OMIM/180700	Online Mendelian Inheritance in Man	CUI