Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

FETAL IODINE DEFICIENCY DISORDER
Synonyms

ENDEMIC CRETINISM
ID

http://purl.bioontology.org/ontology/OMIM/228355
altLabel

ENDEMIC CRETINISM

FIDD
cui

C0342200
MIMTYPEMEANING

Other, mainly phenotypes with suspected mendelian basis
notation

228355
OMIM Entry Type

0
OMIM MimType Value

none
prefLabel

FETAL IODINE DEFICIENCY DISORDER
tui

T047
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http://purl.bioontology.org/ontology/MESH/D003409 Medical Subject Headings CUI
http://purl.bmicc.cn/ontology/ICD10CN/E00 International Classification of Diseases, 10th Edition, China CUI
http://purl.bmicc.cn/ontology/ICD10CN/E00.9 International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/ICD10CM/E00.1 International Classification of Diseases, Version 10 - Clinical Modification CUI