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

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