linear skin defects with multiple congenital anomalies 2

Rare Disease

MONDO:0010474

Also known as:

COX7B microphthalmia with linear skin defects syndromelinear skin defects with multiple congenital anomalies 2linear skin defects with multiple congenital anomalies 2, X-linked dominant

Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the COX7B gene.

Genes

Clinical Trials

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Patient Groups

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Companies Active in linear skin defects with multiple congenital anomalies 2

0 approved

Organizations with approved therapies for this disease

No approved therapies yet

Research is ongoing — 1 company has orphan drug designations for this disease

AGI Dermatics

Other

Designated

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linear skin defects with multiple congenital anomalies 2

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Companies Active in linear skin defects with multiple congenital anomalies 2

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