PCWH syndrome

Summary

PCWH syndrome is a head and neck disease^[1].

Key Facts

• PCWH syndrome's instance of is recorded as head and neck disease^[2].
• PCWH syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• PCWH syndrome's instance of is recorded as rare disease^[4].
• PCWH syndrome's instance of is recorded as class of disease^[5].
• PCWH syndrome is a type of autosomal dominant disease^[6].
• PCWH syndrome is a type of Waardenburg-Shah syndrome^[7].
• PCWH syndrome is a type of genetic peripheral neuropathy^[8].
• PCWH syndrome is a type of pigmentation disorder with eye involvement, excluding albinism^[9].
• PCWH syndrome is a type of rare disease involving intestinal motility^[10].
• PCWH syndrome is a type of leukoderma^[11].
• PCWH syndrome is a type of syndromic genetic deafness^[12].
• PCWH syndrome is a type of syndrome^[13].
• PCWH syndrome's genetic association is recorded as SOX10^[14].
• PCWH syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090111^[15].
• PCWH syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0090111^[16].
• PCWH syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].