Hypopituitarism

Preferred Label : Hypopituitarism;

Inclusion CIM-10 : Necrosis of pituitary gland (postpartum); Lorain-Levi short stature; Kallmann's syndrome; Idiopathic growth hormone deficiency; Panhypopituitarism; Pituitary insufficiency NOS; Isolated deficiency of growth hormone; Isolated deficiency of pituitary hormone; Sheehan's syndrome; Fertile eunuch syndrome; Pituitary cachexia; Pituitary short stature; Hypogonadotropic hypogonadism; Isolated deficiency of gonadotropin; Simmonds' disease;

Diag associé à un acte (%) : 55.3;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E230;

UMLS CUI

C0020635;

Automatic exact mappings (from CISMeF team)
- Gonadotropin deficiency [ICD-11 Subcategory]
- Hypogonadism with anosmia (disorder) [SNOMED CT concept]
- Hypogonadotropic Hypogonadism [NCIt concept]
- Hypogonadotropic Hypogonadism with Anosmia [NCIt concept]
- Hypogonadotropic hypogonadism [HPO term]
- Hypogonadotropic hypogonadism [PASCAL descriptor]
- Hypogonadotropic hypogonadism (disorder) [SNOMED CT concept]
- Hypogonadotropic hypogonadism 23 with or without anosmia [OMIM Phenotype]
- Hypopituitarism, CTCAE [NCIt concept]
- Idiopathic growth hormone deficiency [ICD-11 More detail]
- Idiopathic growth hormone deficiency (disorder) [SNOMED CT concept]
- Isolated gonadotropin deficiency (disorder) [SNOMED CT concept]
- Isolated growth hormone deficiency [OMIM phenotypic series]
- Isolated lutropin deficiency (disorder) [SNOMED CT concept]
- Isolated somatotropin deficiency (disorder) [SNOMED CT concept]
- Kallmann syndrome [ORDO Disease]
- Kallmann syndrome [DO Concept]
- Kallmann syndrome [PASCAL descriptor]
- Kallmann's syndrome [MedDRA LLT]
- Klinefelter Syndrome [NCIt concept]
- Klinefelter syndrome [DO Concept]
- Panhypopituitarism [ICD-11 More detail]
- Panhypopituitarism [NCIt concept]
- Panhypopituitarism [PASCAL descriptor]
- Pituitary cachexia (disorder) [SNOMED CT concept]
- Pituitary hormone deficiency, combined, 2 [OMIM Phenotype]
- Sheehan Syndrome [NCIt concept]
- Sheehan syndrome [ORDO Disease]
- Sheehan syndrome [DO Concept]
- Sheehan syndrome [PASCAL descriptor]
- Sheehan's syndrome [MedDRA LLT]
- Sheehan's syndrome (disorder) [SNOMED CT concept]
- dwarfism, pituitary [MeSH Descriptor]
- hypogonadism [MeSH Descriptor]
- hypogonadotropic hypogonadism [MeSH concept]
- isolated growth hormone deficiency [DO Concept]
- kallmann syndrome [MeSH Descriptor]
- kallmann syndrome [MeSH concept]
- panhypopituitarism [DO Concept]
- postpartum hypopituitarism [MeSH concept]
CISMeF manual mappings
- Non-acquired panhypopituitarism [ORDO Disease]
Currated CISMeF NLP mapping
- Anterior hypopituitarism [HPO term]
- HYPOPITUITARISM [WHO-ART Included Term]
- Hypophyseal insufficiency [PASCAL descriptor]
- Hypopituitalism [MedDRA LLT]
- Hypopituitarism [NCIt concept]
- Hypopituitarism [MedDRA Preferred Term]
- Hypopituitarism [ICD-10 Sub-category (who)]
- Hypopituitarism [ICD-11 Subcategory]
- Hypopituitarism [HPO term]
- Hypopituitarism (disorder) [SNOMED CT concept]
- Insufficiency pituitary [MedDRA LLT]
- PITUITARY INSUFFICIENCY [WHO-ART Preferred Term]
- Panhypopituitarism [MedDRA LLT]
- Panhypopituitarism [HPO term]
- Panhypopituitarism (disorder) [SNOMED CT concept]
- Pituitary insufficiency [MedDRA LLT]
- hypopituitarism [MeSH concept]
- hypopituitarism [MeSH Descriptor]
- hypopituitarism [Disease (Nov.)]
- hypopituitarism [DO Concept]
- hypopituitarism, nos [SNOMED Notion]
- panhypopituitarism, nos [SNOMED Notion]
DO Cross reference
- Kallmann syndrome [DO Concept]
- Sheehan syndrome [DO Concept]
- hypogonadotropic hypogonadism [DO Concept]
- hypogonadotropic hypogonadism 1 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 10 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 11 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 12 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 13 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 14 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 15 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 16 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 17 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 18 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 19 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 2 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 20 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 21 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 22 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 3 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 4 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 5 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 6 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 7 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 8 with or without anosmia [DO Concept]
- hypogonadotropic hypogonadism 9 with or without anosmia [DO Concept]
- hypopituitarism [DO Concept]
- isolated growth hormone deficiency [DO Concept]
- isolated growth hormone deficiency type IA [DO Concept]
- isolated growth hormone deficiency type IB [DO Concept]
- isolated growth hormone deficiency type II [DO Concept]
- isolated growth hormone deficiency type III [DO Concept]
- panhypopituitarism [DO Concept]
Excluded by
- Ovarian dysfunction [ICD-10 category]
- Short stature due to endocrine disorder [ICD-10 Sub-category]
- Testicular dysfunction [ICD-10 category]
Orphanet concepts
- Acquired pituitary hormone deficiency [ORDO Disease]
- Combined pituitary hormone deficiencies, genetic forms [ORDO Disease]
- Congenital hypogonadotropic hypogonadism [ORDO Disease]
- Deficiency in anterior pituitary function-variable immunodeficiency syndrome [ORDO Disease]
- Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome [ORDO Disease]
- Hypopituitarism-micropenis-cleft lip/palate syndrome [ORDO Disease]
- Hypopituitarism-postaxial polydactyly syndrome [ORDO Disease]
- Isolated congenital hypogonadotropic hypogonadism [ORDO Disease]
- Isolated growth hormone deficiency type IA [ORDO Disease]
- Isolated growth hormone deficiency type IB [ORDO Disease]
- Isolated growth hormone deficiency type II [ORDO Disease]
- Isolated growth hormone deficiency type III [ORDO Disease]
- Kallmann syndrome [ORDO Disease]
- Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome [ORDO Disease]
- Non-acquired combined pituitary hormone deficiencies without extrapituitary malformations [ORDO Disease]
- Non-acquired combined pituitary hormone deficiency [ORDO Disease]
- Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome [ORDO Disease]
- Non-acquired isolated growth hormone deficiency [ORDO Disease]
- Non-acquired panhypopituitarism [ORDO Disease]
- Non-acquired pituitary hormone deficiency [ORDO Disease]
- Normosmic congenital hypogonadotropic hypogonadism [ORDO Disease]
- Pituitary deficiency [ORDO Disease]
- Pituitary deficiency due to Rathke cleft cysts [ORDO Disease]
- Pituitary deficiency due to empty sella turcica syndrome [ORDO Disease]
- Pituitary dermoid and epidermoid cysts [ORDO Disease]
- Pituitary hormone deficiency of vascular origin [ORDO Disease]
- Sheehan syndrome [ORDO Disease]
- Short stature due to growth hormone qualitative anomaly [ORDO Disease]
- Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia [ORDO Disease]
- Short stature-pituitary and cerebellar defects-small sella turcica syndrome [ORDO Disease]
- X-linked intellectual disability with isolated growth hormone deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- HYPOPITUITARISM [WHO-ART Included Term]
- Hypopituitalism [MedDRA LLT]
- Hypopituitarism [MedDRA Preferred Term]
- Hypopituitarism [NCIt concept]
- Hypopituitarism [HPO term]
- Hypopituitarism (disorder) [SNOMED CT concept]
- Insufficiency pituitary [MedDRA LLT]
- PITUITARY INSUFFICIENCY [WHO-ART Preferred Term]
- Pituitary deficiency [ORDO Disease]
- Pituitary insufficiency [MedDRA LLT]
- hypopituitarism [MeSH Descriptor]
- hypopituitarism [MeSH concept]
- hypopituitarism [DO Concept]
- hypopituitarism [Disease (Nov.)]
- hypopituitarism, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Sheehan syndrome [ICD-11 More detail]
- hypogonadotropic hypogonadism [DO Concept]
- hypogonadotropic hypogonadism 23 with or without anosmia [DO Concept]

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