Isolated Growth Hormone Deficiency (IGHD)

Isolated Growth Hormone Deficiency(来自ICD-11)

别称:

Non-Acquired Isolated Growth Hormone Deficiency

Congenital Isolated Growth Hormone Deficiency

Congenital Isolated Gh Deficiency

Congenital Ighd

Isolated Somatotropin Deficiency

Dwarfism, Pituitary

Pituitary Dwarfism

Isolated Congenital Growth Hormone Deficiency

Familial Isolated Growth Hormone Deficiency

Isolated Somatotropin Deficiency Disorder

Isolated Human Growth Hormone Deficiency

Dwarfism, Growth Hormone Deficiency

Growth Hormone Deficiency Dwarfism

Isolated Hgh Deficiency

Isolated Gh Deficiency

Dwarfism Pituitary

Ighd

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Isolated Growth Hormone Deficiency, also known as non-acquired isolated growth hormone deficiency, is related to isolated growth hormone deficiency, type ib and isolated growth hormone deficiency type iii. An important gene associated with Isolated Growth Hormone Deficiency is POU1F1 (POU Class 1 Homeobox 1), and among its related pathways/superpathways is Hormonal control of pubertal growth spurt. The drugs Arginine and Hormones have been mentioned in the context of this disorder. Affiliated tissues include pituitary and b cells, and related phenotypes are delayed skeletal maturation and short stature

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