Orphanet: Simpson Golabi Behmel syndrome type 2

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Simpson-Golabi-Behmel syndrome type 2

ORPHA:79022

Classification level: Disorder

Synonym(s):
- Lethal variant of Simpson-Golabi-Behmel syndrome
- SGBS2
Prevalence: -
Inheritance: -
Age of onset: -
ICD-10: -
OMIM: -
UMLS: C1846175
MeSH: -
GARD: -
MedDRA: -

Summary

This disease has been moved to Multiple congenital anomalies-hypotonia-seizures syndrome type 2

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