All
 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