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Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia

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ORPHA:632

Classification level: Subtype of disorder

Prevalence: -

Inheritance: X-linked recessive

Age of onset: Infancy, Neonatal

ICD-10: E23.0

ICD-11: 4A01.00

OMIM: 307200

UMLS: C0472813

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.

Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

Guidelines
Emergency guidelines
Français (2020.pdf) - Orphanet Urgences
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