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non-acquired combined pituitary hormone deficiency

^ http://purl.obolibrary.org/obo/MONDO_0018762

Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. [ Orphanet:467 ]

Term info

database cross reference
  • ICD10CM:E23.0 (Orphanet:467/ntbt)
  • Orphanet:467 (MONDO:equivalentTo)
Subsets

disease_grouping, ordo_group_of_disorders

definition

Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis.

exactMatch

http://purl.obolibrary.org/obo/Orphanet_467

has exact synonym

congenital hypopituitarism, congenital combined pituitary hormone deficiency

id

MONDO:0018762

Term relations