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Online Mendelian Inheritance in Man
Last uploaded:
January 16, 2025
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Id | http://purl.bioontology.org/ontology/OMIM/228355
http://purl.bioontology.org/ontology/OMIM/228355
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Preferred Name | FETAL IODINE DEFICIENCY DISORDER |
Synonyms |
FIDD
ENDEMIC CRETINISM
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
altLabel |
FIDD
ENDEMIC CRETINISM
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prefLabel |
FETAL IODINE DEFICIENCY DISORDER
|
notation |
228355
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OMIM MimType Value |
none
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Semantic type UMLS property | |
OMIM Entry Type |
0
|
type | |
MIMTYPEMEANING |
Other, mainly phenotypes with suspected mendelian basis
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tui |
T047
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cui |
C0342200
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