5A61.0
category
Hypopituitarism
Definition
A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/infarction.
Inclusions
- pituitary cachexia
- pituitary short stature
Also indexed as
Acquired hypopituitarismAdenohypophysis deficiency with or without pituitary stalk interruption syndrome (PSIS)Amenorrhoea-hyperprolactinaemia syndromeAnosmic congenital hypogonadotropic hypogonadismAutoimmune hypopituitarismBBS - [Bardet-Biedl syndrome]Bardet-Biedl syndromeBrissaud's infantilism or dwarfismCHARGE associationCHARGE syndromeCataract - intellectual deficit - hypogonadismChoanal atresia, Coloboma, Characteristic ears and Cranial nerve anomaliesColoboma, Heart defect, Atresia choanae, Retarded growth and development, Genital hypoplasia, Ear anomalies/deafnessComplete growth hormone insensitivityCongenital IGHD - [isolated growth hormone deficiency]Congenital hypogonadotropic hypogonadismCongenital hypogonadotropic hypogonadism with anosmiaCongenital isolated growth hormone deficiencyDe Morsier syndromeDiabetes - hypogonadism - deafness - intellectual deficitDrug-induced hypopituitarismEctopic neurohypophysisFemale infertility associated with pituitary-hypothalamic originFertile eunuch syndromeGHIS - [Growth hormone insensitivity syndrome]Genetic growth hormone deficiencyGranulomatous hypophysitisGrowth delay - deafness- intellectual deficitGrowth delay due to insulin-like growth factor I deficiencyGrowth delay due to insulin-like growth factor I resistanceGrowth hormone deficiency with or without PSIS - [pituitary stalk interruption syndrome]Growth hormone deficiency with or without pituitary stalk interruption syndromeGrowth hormone insensitivity syndromeGrowth hormone receptor deficiencyHypogonadotropic hypogonadism associated with other endocrinopathiesHypophysitisHypopituitarismHypopituitarism due to a granulomatous diseaseHypopituitarism due to a metabolic diseaseHypopituitarism secondary to a granulomatous diseaseHypopituitarism secondary to a metabolic diseaseIGF-1 - [ insulin-like growth factor I] deficiencyIdiopathic growth hormone deficiencyIdiopathic hypopituitarismIgG4-related hypophysitisInfantilism syndromeInfectious hypopituitarismIschaemic pituitary necrosisIschaemic postpartum pituitary necrosisIsolated FSH deficiencyIsolated congenital gonadotropin deficiencyIsolated deficiency of pituitary hormoneIsolated follicle stimulating hormone deficiencyIsolated luteinising hormone deficiencyIsolated lutropin deficiencyIsolated somatotropin deficiencyKallmann syndromeKowarski syndromeLaron syndromeLaron syndrome with immunodeficiencyLaron-type dwarfismLate-onset isolated ACTH deficiencyLate-onset isolated adrenocorticotropin deficiencyLorain dwarfismLorain infantilismLorain-Levi dwarfismLymphocytic hypophysitisMyopathy in hypopituitarismNanism due to growth hormone qualitative anomalyNecrosis of pituitary glandNon-acquired combined pituitary deficiencyNon-acquired pituitary deficiencyNonacquired combined hypopituitarismNonacquired hypopituitarismNonacquired isolated growth hormone deficiencyNormosmic congenital hypogonadotropic hypogonadismOlfactogenital dysplasiaPSIS - [pituitary stalk interruption syndrome]PanhypopituitarismPineal germinomaPituitary apoplexyPituitary deficiency due to Rathke pouch cystsPituitary deficiency due to empty sella turcica syndromePituitary dermoid or epidermoid cystsPituitary nanismPituitary stalk interruption syndromePostpartum pituitary necrosisPrimary GH resistancePrimary growth hormone insensitivityPrimary growth hormone resistancePrimary insulin-like growth factor deficiencyResistance to IGF-1 - [ insulin-like growth factor I]SOD - [Septo-optic dysplasia]Secondary hypopituitarismSepto-optic dysplasiaSeptooptic dysplasia spectrumSheehan diseaseSheehan syndromeShort stature due to a defect in growth hormone receptor or post receptor pathwayShort stature due to growth hormone qualitative anomalyShort stature due to growth hormone resistanceShort stature due to primary acid-labile subunit deficiencySimmonds SyndromeSuprasellar germinomaSyndrome with hypogonadotropic hypogonadismTraumatic hypopituitarismTumoural hypopituitarismVascular hypopituitarismWSS - [Woodhouse-Sakati syndrome]Woodhouse-Sakati syndromeX-linked intellectual deficit with isolated growth hormone deficiencyXanthomatous hypophysitisanosmia eunuchoidismanterior pituitary hypofunctionanterior pituitary insufficiency (in part)deficient secretion of all pituitary hormonesdeficient secretion of one or more pituitary hormonesdrug hypopituitarismdysplasia olfactogenitalis of de Morsiergonadotrophin deficiency with anosmiagrowth hormone insufficiencyhypogonadotropic eunuchoidismhypohypophysismhypophyseal dwarfismhypophyseal dystrophyhypophyseal short staturehypopituitarism syndromehypopituitary cachexiahypopituitary dwarfismhyposomatotropic dwarfismisolated deficiency of [HGH] - human growth hormoneisolated deficiency of growth hormoneisolated gonadotrophin deficiencyisolated growth hormone insufficiencyjuvenile hypopituitarismmedicament-induced hypopituitarismpanhypopituitarism syndromepituitary cachexiapituitary deficiencypituitary dwarfismpituitary failurepituitary gland hypofunctionpituitary hormone deficiencypituitary hypoadrenocorticismpituitary hypofunctionpituitary hypogonadismpituitary infantilismpituitary insufficiency NOSpituitary short staturepostpartum hypopituitarismpostpartum necrosis of pituitary glandpostpartum panhypopituitary syndromeprepubertal dwarfismprepubertal panhypopituitarismprimary hypopituitarismsecondary hypogonadismsepto-optic dysplasia sequencesomatotropin deficiencysubpituitarism