Congenital intestinal motility disorder Neurologic Waardenburg-Shah syndrome PCWH Peripheral demyelinating neuropathy - central dysmyelinating leukodystrophy - Waardenburg syndrome - Hirschsprung disease WS4 plus OMIM:609136 ICD10:E75.2 Genetic hypopigmentation of the skin Genetic digestive tract malformation Rare genetic neurological disorder Syndromic genetic deafness Pigmentation disorder with eye involvement, excluding albinism