Preferred Name | congenital hypothyroidism | |
Synonyms |
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|
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 SNOMEDCT_US_2023_03_01:217710005 MESH:D003409 ICD10CM:E03.1 UMLS_CUI:C0342200 UMLS_CUI:C0010308 SNOMEDCT_US_2023_03_01:75065003 OMIM:PS275200 GARD:1487 ICD9CM:243 NCI:C26734 NCI:C98921 |
|
definition |
A hypothyroidism that is present at birth. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
disease has basis in | ||
has_alternative_id |
DOID:11631 DOID:11632 |
|
has_obo_namespace |
disease_ontology |
|
id |
DOID:0050328 |
|
in_subset | ||
label |
congenital hypothyroidism |
|
notation |
DOID:0050328 |
|
note |
A hypothyroidism that is present at birth. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
preferred label |
congenital hypothyroidism |
|
prefLabel |
congenital hypothyroidism |
|
subClassOf |
Create mapping