linear skin defects with multiple congenital anomalies 1
A syndromic microphthalmia characterized by unilateral or bilateral microphthalmia and linear skin defects on the face and neck in females and in utero lethality in males that has_material_basis_in heterozygous or hemizygous mutation in the HCCS gene on chromosome Xp22.2. (DO)
linear skin defects with multiple congenital anomalies 2
linear skin defects with multiple congenital anomalies 3