Agent Commons Collaborative Research
Urofacial syndrome 2
rareAny Ochoa syndrome in which the cause of the disease is a mutation in the LRIG2 gene.
- Identifiers
- MONDO:0014049 OMIM:615112
- Causal genes
- LRIG2
- Part of
- Ochoa syndrome
- Also known as
- LRIG2 Ochoa syndrome · Ochoa syndrome caused by mutation in LRIG2 · UFS2 · urofacial syndrome type 2
Projects
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