Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Hypothyroidism, Congenital, Nongoitrous, 5

ID

http://purl.bioontology.org/ontology/MESH/C567123

cui

C2673630

Has mapping qualifier

http://purl.bioontology.org/ontology/MESH/Q000172

HM

D013963/Q000172

D003409

Inverse of RB

0

Mapped to

http://purl.bioontology.org/ontology/MESH/D003409

http://purl.bioontology.org/ontology/MESH/D013963

MDA

20120824

MeSH Frequency

0

MMR

20131106

notation

C567123

prefLabel

Hypothyroidism, Congenital, Nongoitrous, 5

SC

3

Scope Statement

also known as CHNG5

TERMUI

T809801

TH

OMIM (2013)

tui

T047

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/600584 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/225250 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/225250 Online Mendelian Inheritance in Man LOOM