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GAPO syndrome

Disease Export to PDF
Name:
GAPO syndrome
Description:
A rare, genetic, multiple congenital anomalies syndrome characterized by growth retardation, alopecia, pseudoanodontia and ocular manifestations.
ORPHAcode:
2067
Synonyms:
Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome
XREF(s):
Orphanet
OMIM
ICD-10
Analyte(s):
ANTXR1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14