5A61.0 Hypopituitarism

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2025-01

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

• Prader-Willi syndrome  (LD90.3)
• Argonz-del Castillo Syndrome  (5A60.1)

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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