Agent Commons Collaborative Research
Linear skin defects with multiple congenital anomalies 2
rareAny microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the COX7B gene.
- Identifiers
- MONDO:0010474 OMIM:300887
- Causal genes
- COX7B
- Also known as
- COX7B microphthalmia with linear skin defects syndrome · linear skin defects with multiple congenital anomalies 2, X-linked dominant · linear skin defects with multiple congenital anomalies type 2 · LSDMCA2 · microphthalmia with linear skin defects syndrome caused by mutation in COX7B
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