Preferred Name |
congenital hypothyroidism |
|
Synonyms |
|
|
Definitions |
A hypothyroidism that is present at birth. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
ID |
http://purl.obolibrary.org/obo/DOID_0050328 |
|
comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
database_cross_reference |
ICD10CM:E00.1 MESH:D003409 ICD10CM:E03.1 UMLS_CUI:C0342200 UMLS_CUI:C0010308 SNOMEDCT_US_2020_03_01:75065003 SNOMEDCT_US_2020_03_01:217710005 OMIM:PS275200 GARD:1487 ICD9CM:243 NCI:C26734 NCI:C98921 |
|
has_alternative_id |
DOID:11631 DOID:11632 |
|
has_obo_namespace |
disease_ontology |
|
id |
DOID:0050328 |
|
imported from | ||
in_subset | ||
label |
congenital hypothyroidism |
|
notation |
DOID:0050328 |
|
prefLabel |
congenital hypothyroidism |
|
textual definition |
A hypothyroidism that is present at birth. |
|
subClassOf |
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