Skin Diseases, Genetic (medical concept explorer)

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Medical Concepts

Diseases

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Genetic Diseases, Inborn

Adrenal Hyperplasia, Congenital

Alagille Syndrome

alpha 1-Antitrypsin Deficiency

Anemia, Hemolytic, Congenital

Anemia, Hypoplastic, Congenital

Angioedemas, Hereditary

Ataxia Telangiectasia

Autoimmune Lymphoproliferative Syndrome

Blood Coagulation Disorders, Inherited

Brugada Syndrome

Camurati-Engelmann Syndrome

Cardiomyopathy, Hypertrophic, Familial

CHARGE Syndrome

Chromosome Disorders

Costello Syndrome

Cystic Fibrosis

Donohue Syndrome

Eye Diseases, Hereditary

Frasier Syndrome

Genetic Diseases, X-Linked

Genetic Diseases, Y-Linked

Hajdu-Cheney Syndrome

Hemoglobinopathies

Hereditary Autoinflammatory Diseases

Heredodegenerative Disorders, Nervous System

Hyperthyroxinemia, Familial Dysalbuminemic

Kallmann Syndrome

Kartagener Syndrome

Loeys-Dietz Syndrome

Marfan Syndrome

Metabolism, Inborn Errors

Muscular Dystrophies

Myasthenic Syndromes, Congenital

Nail-Patella Syndrome

Neoplastic Syndromes, Hereditary

Osteogenesis Imperfecta

Pain Insensitivity, Congenital

Pelger-Huet Anomaly

Polycystic Kidney, Autosomal Recessive

Pycnodysostosis

Skin Diseases, Genetic

Dermatitis, Atopic

Dyskeratosis Congenita

Ectodermal Dysplasia

Ehlers-Danlos Syndrome

Epidermolysis Bullosa

Erythrokeratodermia Variabilis

Hyalinosis, Systemic

Ichthyosiform Erythroderma, Congenital

Ichthyosis Bullosa of Siemens

Ichthyosis Vulgaris

Ichthyosis, X-Linked

Incontinentia Pigmenti

Keratoderma, Palmoplantar

Leukokeratosis, Hereditary Mucosal

Lipoid Proteinosis of Urbach and Wiethe

Netherton Syndrome

Pemphigus, Benign Familial

Porphyria, Erythropoietic

Porphyrias, Hepatic

Prolidase Deficiency

Pseudoxanthoma Elasticum

Rothmund-Thomson Syndrome

Sjogren-Larsson Syndrome

Trichothiodystrophy Syndromes

Xeroderma Pigmentosum

Weill-Marchesani Syndrome

Werner Syndrome

Yellow Nail Syndrome

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