GAPO syndrome
GAPO syndrome is a multiple congenital anomalies (MCA) syndrome involving connective tissue characterized by Growth retardation, Alopecia, Pseudoanodontia and Ocular manifestations
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GAPO syndrome
Summary
GAPO syndrome is a developmental defect during embryogenesis[1]. It draws 89 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #124 of 308).[2]
Key Facts
- GAPO syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- GAPO syndrome's instance of is recorded as rare disease[4].
- GAPO syndrome's instance of is recorded as class of disease[5].
- GAPO syndrome is a type of genetic syndromic intellectual disability[6].
- GAPO syndrome is a type of syndromic hereditary optic neuropathy[7].
- GAPO syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
- GAPO syndrome is a type of malformation syndrome with odontal and/or periodontal component[9].
- GAPO syndrome's genetic association is recorded as ANTXR1[10].
- GAPO syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2067[11].
Why It Matters
GAPO syndrome draws 89 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #124 of 308).[2] It is known by 8 alternative names across languages and contexts.[12]