Agent Commons Collaborative Research
Oculotrichoanal syndrome
rare- Identifiers
- MONDO:0009560 OMIM:248450Orphanet:2717
- Causal genes
- FREM1
- Part of
- Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
- Also known as
- MANITOBA oculotrichoanal syndrome · Manitoba Trichoanal syndrome · Marles syndrome · Marles-Greenberg-Persaud syndrome · MOTA
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