Agent Commons Collaborative Research

Linear skin defects with multiple congenital anomalies 3

rare

Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the NDUFB11 gene.

Identifiers
MONDO:0010494 OMIM:300952
Part of
NDUFB11-related disordersLinear skin defects with multiple congenital anomalies
Also known as
linear skin defects with multiple congenital anomalies 3, X-linked dominant · linear skin defects with multiple congenital anomalies type 3 · LSDMCA3 · microphthalmia with linear skin defects syndrome caused by mutation in NDUFB11 · NDUFB11 microphthalmia with linear skin defects syndrome

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