Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Branchial Cleft Anomalies

ID

http://purl.bioontology.org/ontology/MESH/C562384

cui

C0079037

Has mapping qualifier

http://purl.bioontology.org/ontology/MESH/Q000002

HM

D019465

D010608

D001934/Q000002

Inverse of RB

0

Mapped to

http://purl.bioontology.org/ontology/MESH/D019465

http://purl.bioontology.org/ontology/MESH/D010608

http://purl.bioontology.org/ontology/MESH/D001934

MDA

20121105

MeSH Frequency

49

MMR

20150817

notation

C562384

prefLabel

Branchial Cleft Anomalies

SC

3

Scope Statement

Congenital abnormalities of the neck that include CYSTS, sinuses, or FISTULAS which connect the skin and PHARYNX. Autosomal dominant inheritance has been observed. OMIM: 113600

TERMUI

T800592

TH

OMIM (2013)

tui

T019

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/113600 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/113600 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q18.2 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/MTHU016602 Online Mendelian Inheritance in Man CUI