linear skin defects with multiple congenital anomalies 3

Rare Disease

MONDO:0010494

Also known as:

NDUFB11 microphthalmia with linear skin defects syndromelinear skin defects with multiple congenital anomalies 3linear skin defects with multiple congenital anomalies 3, X-linked dominant

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

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Companies Active in linear skin defects with multiple congenital anomalies 3

1 company

Organizations with orphan designations or approved therapies for this disease

AGI Dermatics

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