Isolated Growth Hormone Deficiency Type Iii

Isolated Growth Hormone Deficiency Type Iii(来自ICD-11)

别称:

Congenital Isolated Growth Hormone Deficiency Type Iii

X-Linked Isolated Growth Hormone Deficiency

Congenital Isolated Gh Deficiency Type Iii

Congenital Ighd Type Iii

X-Linked Ighd

Growth Hormone Deficiency with Hypogammaglobulinemia

X-Linked Hypogammaglobulinemia and Isolated Growth Hormone Deficiency

X-Linked Agammaglobulinemia and Isolated Growth Hormone Deficiency

X-Linked Agammaglobulinemia with Growth Hormone Deficiency

Isolated Growth Hormone Deficiency, Type Iii

Fleisher Syndrome

Ighd Iii

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Isolated Growth Hormone Deficiency Type Iii, also known as congenital isolated growth hormone deficiency type iii, is related to isolated growth hormone deficiency and growth hormone deficiency, and has symptoms including diarrhea An important gene associated with Isolated Growth Hormone Deficiency Type Iii is BTK (Bruton Tyrosine Kinase), and among its related pathways/superpathways are Akt Signaling and PAK Pathway. Affiliated tissues include pituitary and b cells, and related phenotypes are Increased shRNA abundance (Z-score > 2) and growth/size/body region

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