5A61.0 Hypopituitarism
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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
code elsewhere
synonyms
- Hypopituitarism
- subpituitarism
- hypophyseal dystrophy
- hypohypophysism
- anterior pituitary insufficiency (in part)
- deficient secretion of one or more pituitary hormones
- hypopituitarism syndrome
- pituitary deficiency
- pituitary failure
- pituitary hypofunction
- pituitary insufficiency NOS
- anterior pituitary hypofunction
- deficient secretion of all pituitary hormones
- hypopituitary dwarfism
- hyposomatotropic dwarfism
- hypophyseal dwarfism
- hypopituitary cachexia
- hypophyseal short stature
- panhypopituitarism syndrome
- pituitary cachexia
- juvenile hypopituitarism
- pituitary dwarfism
- pituitary gland hypofunction
- primary hypopituitarism
- secondary hypogonadism
- prepubertal panhypopituitarism
- prepubertal dwarfism
- postpartum panhypopituitary syndrome
- postpartum hypopituitarism
- pituitary short stature
- pituitary infantilism
- pituitary hypogonadism
- pituitary hypoadrenocorticism
- Nonacquired hypopituitarism
- Non-acquired pituitary deficiency
- Isolated FSH deficiency
- Isolated follicle stimulating hormone deficiency
- Nonacquired combined hypopituitarism
- Non-acquired combined pituitary deficiency
- Adenohypophysis deficiency with or without pituitary stalk interruption syndrome (PSIS)
- Panhypopituitarism
- Septo-optic dysplasia
- Septooptic dysplasia spectrum
- De Morsier syndrome
- septo-optic dysplasia sequence
- SOD - [Septo-optic dysplasia]
- Nonacquired isolated growth hormone deficiency
- Congenital isolated growth hormone deficiency
- Pituitary nanism
- Congenital IGHD - [isolated growth hormone deficiency]
- Growth hormone deficiency with or without pituitary stalk interruption syndrome
- Growth hormone deficiency with or without PSIS - [pituitary stalk interruption syndrome]
- Genetic growth hormone deficiency
- X-linked intellectual deficit with isolated growth hormone deficiency
- Idiopathic growth hormone deficiency
- growth hormone insufficiency
- isolated deficiency of growth hormone
- isolated growth hormone insufficiency
- isolated deficiency of [HGH] - human growth hormone
- Short stature due to growth hormone qualitative anomaly
- Nanism due to growth hormone qualitative anomaly
- Kowarski syndrome
- Pituitary stalk interruption syndrome
- Ectopic neurohypophysis
- PSIS - [pituitary stalk interruption syndrome]
- Short stature due to a defect in growth hormone receptor or post receptor pathway
- Growth hormone insensitivity syndrome
- GHIS - [Growth hormone insensitivity syndrome]
- Growth delay due to insulin-like growth factor I deficiency
- Primary insulin-like growth factor deficiency
- Growth delay - deafness- intellectual deficit
- IGF-1 - [ insulin-like growth factor I] deficiency
- Growth delay due to insulin-like growth factor I resistance
- Resistance to IGF-1 - [ insulin-like growth factor I]
- Short stature due to growth hormone resistance
- Complete growth hormone insensitivity
- Primary growth hormone insensitivity
- Growth hormone receptor deficiency
- Primary growth hormone resistance
- Primary GH resistance
- Laron-type dwarfism
- Laron syndrome
- Short stature due to primary acid-labile subunit deficiency
- Laron syndrome with immunodeficiency
- Congenital hypogonadotropic hypogonadism
- Anosmic congenital hypogonadotropic hypogonadism
- Congenital hypogonadotropic hypogonadism with anosmia
- hypogonadotropic eunuchoidism
- anosmia eunuchoidism
- dysplasia olfactogenitalis of de Morsier
- gonadotrophin deficiency with anosmia
- Normosmic congenital hypogonadotropic hypogonadism
- Isolated congenital gonadotropin deficiency
- isolated gonadotrophin deficiency
- Syndrome with hypogonadotropic hypogonadism
- Bardet-Biedl syndrome
- BBS - [Bardet-Biedl syndrome]
- Cataract - intellectual deficit - hypogonadism
- CHARGE syndrome
- Coloboma, Heart defect, Atresia choanae, Retarded growth and development, Genital hypoplasia, Ear anomalies/deafness
- Choanal atresia, Coloboma, Characteristic ears and Cranial nerve anomalies
- CHARGE association
- Woodhouse-Sakati syndrome
- Diabetes - hypogonadism - deafness - intellectual deficit
- Hypogonadotropic hypogonadism associated with other endocrinopathies
- Acquired hypopituitarism
- Secondary hypopituitarism
- Drug-induced hypopituitarism
- drug hypopituitarism
- medicament-induced hypopituitarism
- Tumoural hypopituitarism
- Infectious hypopituitarism
- Autoimmune hypopituitarism
- Vascular hypopituitarism
- Sheehan syndrome
- Sheehan disease
- Hypopituitarism due to a metabolic disease
- Hypopituitarism secondary to a metabolic disease
- Hypopituitarism due to a granulomatous disease
- Hypopituitarism secondary to a granulomatous disease
- Traumatic hypopituitarism
- Hypophysitis
- Lymphocytic hypophysitis
- Granulomatous hypophysitis
- IgG4-related hypophysitis
- Xanthomatous hypophysitis
- Pineal germinoma
- Suprasellar germinoma
- Pituitary deficiency due to Rathke pouch cysts
- Pituitary dermoid or epidermoid cysts
- Pituitary deficiency due to empty sella turcica syndrome
- Pituitary apoplexy
- Late-onset isolated ACTH deficiency
- Late-onset isolated adrenocorticotropin deficiency
- Idiopathic hypopituitarism
- Simmonds Syndrome
- Amenorrhoea-hyperprolactinaemia syndrome
- Brissaud's infantilism or dwarfism
- Female infertility associated with pituitary-hypothalamic origin
- Fertile eunuch syndrome
- Infantilism syndrome
- Ischaemic pituitary necrosis
- Ischaemic postpartum pituitary necrosis
- Isolated deficiency of pituitary hormone
- pituitary hormone deficiency
- Isolated lutropin deficiency
- Isolated luteinising hormone deficiency
- Isolated somatotropin deficiency
- somatotropin deficiency
- Lorain dwarfism
- Lorain infantilism
- Lorain-Levi dwarfism
- Necrosis of pituitary gland
- Postpartum pituitary necrosis
- postpartum necrosis of pituitary gland
- Myopathy in hypopituitarism
- Olfactogenital dysplasia
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