Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024

Preferred Name	FETAL IODINE DEFICIENCY DISORDER
Synonyms	FIDD
ID	http://purl.bioontology.org/ontology/OMIM/228355
altLabel	FIDD ENDEMIC CRETINISM
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

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/SNMI/D4-01836	SNMI	CUI
http://purl.bioontology.org/ontology/RCD/X40I8	RCD	CUI
http://purl.bioontology.org/ontology/ICD10CM/E00.1	ICD10CM	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/75065003	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/SCTSPA/75065003	SCTSPA	CUI
http://purl.bioontology.org/ontology/SNMI/D4-01830	SNMI	CUI
http://purl.bioontology.org/ontology/MSHFRE/D003409	MSHFRE	CUI
http://purl.bioontology.org/ontology/RCD/X40I6	RCD	CUI
http://purl.bioontology.org/ontology/MESH/D003409	MESH	CUI