isolated growth hormone deficiency type III (Q32136664)
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An isolated growth hormone deficiency characterized by dwarfism, variable occurence of hypogammaglobulinemia, and a generally good response to growth hormone therapy that has material basis in mutation in the BTK gene on chromosome Xq22.1.
- congenital isolated growth hormone deficiency type III
- Fleisher syndrome
- X-linked agammaglobulinemia and isolated growth hormone deficiency
- congenital isolated GH deficiency type III
- X-linked isolated growth hormone deficiency
- growth hormone deficiency with hypogammaglobulinemia
- X-linked IGHD
- IGHD III
- X-linked hypogammaglobulinemia and isolated growth hormone deficiency
- congenital IGHD type III
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | isolated growth hormone deficiency type III |
An isolated growth hormone deficiency characterized by dwarfism, variable occurence of hypogammaglobulinemia, and a generally good response to growth hormone therapy that has material basis in mutation in the BTK gene on chromosome Xq22.1. |
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