Biological Sciences and Healthcare, part 4

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > disease > Disease of head > Disorder of ear > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Disease of head > Disorder of ear > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Finding of head region > Ear finding > Disorder of ear > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > disease > ear, nose and throat disorder > Disorder of ear > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > disease > Congenital disease > Congenital malformation > Congenital malformation syndrome (disorder) > Multiple system malformation syndrome > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > disease > developmental disorder > Congenital malformation > Congenital malformation syndrome (disorder) > Multiple system malformation syndrome > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > Skin AND/OR mucosa finding (finding) > Skin finding > Disease of skin > Skin lesion > Anomalous pigmentation of skin > Genetic disorder of skin pigmentation (disorder) > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Disease of skin AND/OR subcutaneous tissue > Disease of skin > Skin lesion > Anomalous pigmentation of skin > Genetic disorder of skin pigmentation (disorder) > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > Skin AND/OR mucosa finding (finding) > Skin or mucosa lesion > Lesion of skin and/or skin-associated mucous membrane > Skin lesion > Anomalous pigmentation of skin > Genetic disorder of skin pigmentation (disorder) > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > disease > Disorder of pigmentation (disorder) > Anomalous pigmentation of skin > Genetic disorder of skin pigmentation (disorder) > Waardenburg's syndrome > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Bowel finding > Disease of intestine > Congenital anomaly of intestinal tract > Congenital anomaly of large intestine > Aganglionosis of large intestine (disorder) > Aganglionic megacolon > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > disease > Disorder of body system > Disease of nervous system > Disorder of autonomic nervous system > Congenital malformation of autonomic nervous system (disorder) > Aganglionosis of large intestine (disorder) > Aganglionic megacolon > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

Motility disorder of large intestine > Aganglionic megacolon > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)

... > Clinical finding (finding) > disease > Disorder of body system > Disease of nervous system > Disorder of autonomic nervous system > Inherited autonomic nervous system disorder (disorder) > Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder)