JSON

non-acquired combined pituitary hormone deficiency

Go to external page 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 ]

Synonyms: congenital hypopituitarism congenital combined pituitary hormone deficiency

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C5680091 (MONDO:equivalentTo)
  • MEDGEN:1842250 (MONDO:equivalentTo)
  • Orphanet:467 (MONDO:equivalentTo)
  • GARD:2252 (MONDO:GARD)
  • ICD10CM:E23.0 (Orphanet:467/ntbt)
  • NANDO:2200312 (https://orcid.org/0000-0003-0011-764X)
Subsets

gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders

exactMatch

http://linkedlifedata.com/resource/umls/id/C5680091

http://www.orpha.net/ORDO/Orphanet_467

http://identifiers.org/medgen/1842250

id

MONDO:0018762

Term relations