Search Ontology:

Human Disease

congenital hypothyroidism

Term ID

DOID:0050328

Synonyms

Definition

A hypothyroidism that is present at birth. (2)

References

GARD:1487
ICD10CM:E00.1
ICD10CM:E03.1
ICD9CM:243
MESH:D003409
MIM:PS275200
NCI:C26734
NCI:C98921
SNOMEDCT_US_2023_03_01:217710005
SNOMEDCT_US_2023_03_01:75065003
UMLS_CUI:C0010308
UMLS_CUI:C0342200

Ontology

Human Disease ( DOID:0050328 )

Relationships

is a type of: hypothyroidism physical disorder

hypothyroidism physical disorder Show first 5 Terms
has subtype: congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 ... Show All 10 Terms

congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nongoitrous hypothyroidism 7 congenital nongoitrous hypothyroidism 8 congenital nongoitrous hypothyroidism 9 familial thyroid dyshormonogenesis Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models