Linear skin defects with multiple congenital anomalies 1

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

Also known as: HCCS microphthalmia with linear skin defects syndrome, linear skin defects with multiple congenital anomalies 1, linear skin defects with multiple congenital anomalies 1, X-linked dominant, microphthalmia with linear skin defects syndrome caused by mutation in HCCS, LSDMCA1, Midas syndrome, microphthalmia with linear skin defects, microphthalmia, dermal aplasia, and sclerocornea

16 clinical trials for this condition and its sub-types.