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Isolated growth hormone deficiency type III
ORPHA:231692
Classification level: Subtype of disorder- Synonym(s):
- Congenital IGHD type III
- Congenital isolated GH deficiency type III
- Congenital isolated growth hormone deficiency type III
- X-linked IGHD
- X-linked isolated growth hormone deficiency
- Prevalence: -
- Inheritance: X-linked recessive
- Age of onset: Infancy, Neonatal
- ICD-10: E23.0
- OMIM: 300123 307200
- UMLS: -
- MeSH: -
- GARD: 3921
- MedDRA: -
Summary
An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.
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