About: Congenital Hypothyroidism     Goto   Sponge   Distinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Congenital Hypothyroidism
rdfs:subClassOf
Has_NICHD_Parent
Concept_In_Subset
Semantic_Type
  • Congenital Abnormality
  • Disease or Syndrome
Preferred_Name
  • Congenital Hypothyroidism
UMLS_CUI
  • C0010308
Contributing_Source
  • NICHD
ALT_DEFINITION
  • A condition due to congenital lack of thyroid hormone, marked by arrested physical and mental development, dystrophy of the bones and soft parts, and lowered basal metabolism. It is the congenital form of thyroid deficiency, while MYXEDEMA is the acquired form. (From Dorland, 27th ed)MSH2003_2003_05_12
Legacy_Concept_Name
  • Congenital_Hypothyroidism
FULL_SYN
  • Congenital HypothyroidismPTNCI
  • Congenital HypothyroidismPTNICHD
DEFINITION
  • A deficiency of thyroid hormone present at birth. The etiology can be genetic or environmental, or a combination of both; treatment is based on severity and causality.NCI
code
  • C26734
is rdfs:subClassOf of
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