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 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.850 Skin Diseases, Genetic D012873 +
     C16.320.850.080 Albinism D000417 +
     C16.320.850.180 Cutis Laxa D003483 
     C16.320.850.210 Dermatitis, Atopic D003876 
     C16.320.850.250 Ectodermal Dysplasia D004476 +
     C16.320.850.260 Ehlers-Danlos Syndrome D004535 
     C16.320.850.275 Epidermolysis Bullosa D004820 +
     C16.320.850.420 Incontinentia Pigmenti D007184 
     C16.320.850.490 Keratosis Follicularis D007644 
     C16.320.850.475 Keratoderma, Palmoplantar D007645 +
     C16.320.850.715 Poikiloderma Congenitale D011038 
     C16.320.850.750 Pseudoxanthoma Elasticum D011561 
     C16.320.850.970 Xeroderma Pigmentosum D014983 
     C16.320.850.820 Sjogren-Larsson Syndrome D016111 
     C16.320.850.405 Ichthyosis Vulgaris D016112 
     C16.320.850.400 Ichthyosiform Erythroderma, Congenital D016113 +
     C16.320.850.408 Ichthyosis, X-Linked D016114 
     C16.320.850.700 Pemphigus, Benign Familial D016506 
     C16.320.850.738 Porphyria, Erythropoietic D017092 
     C16.320.850.742 Porphyria, Hepatic D017094 +
     C16.320.850.735 Porphyria, Erythrohepatic D017121 
     C16.320.850.730 Porokeratosis D017499 
     C16.320.850.235 Dyskeratosis Congenita D019871 

 C17 Skin and Connective Tissue Diseases D017437 +
  C17.800 Skin Diseases D012871 +
   C17.800.827 Skin Diseases, Genetic D012873 +
     C17.800.827.080 Albinism D000417 +
     C17.800.827.180 Cutis Laxa D003483 
     C17.800.827.210 Dermatitis, Atopic D003876 
     C17.800.827.250 Ectodermal Dysplasia D004476 +
     C17.800.827.260 Ehlers-Danlos Syndrome D004535 
     C17.800.827.275 Epidermolysis Bullosa D004820 +
     C17.800.827.420 Incontinentia Pigmenti D007184 
     C17.800.827.490 Keratosis Follicularis D007644 
     C17.800.827.475 Keratoderma, Palmoplantar D007645 +
     C17.800.827.715 Poikiloderma Congenitale D011038 
     C17.800.827.750 Pseudoxanthoma Elasticum D011561 
     C17.800.827.970 Xeroderma Pigmentosum D014983 
     C17.800.827.820 Sjogren-Larsson Syndrome D016111 
     C17.800.827.405 Ichthyosis Vulgaris D016112 
     C17.800.827.400 Ichthyosiform Erythroderma, Congenital D016113 +
     C17.800.827.408 Ichthyosis, X-Linked D016114 
     C17.800.827.700 Pemphigus, Benign Familial D016506 
     C17.800.827.738 Porphyria, Erythropoietic D017092 
     C17.800.827.742 Porphyria, Hepatic D017094 +
     C17.800.827.735 Porphyria, Erythrohepatic D017121 
     C17.800.827.730 Porokeratosis D017499 
     C17.800.827.235 Dyskeratosis Congenita D019871