Skin Diseases | Page 1

A Diseases

Aagenaes syndrome Aarskog syndrome Abdominal chemodectomas with cutaneous angiolipomas Absence of fingerprints congenital milia Acanthosis nigricans Acquired generalized lipodystrophy Acral peeling skin syndrome Acrodermatitis Acrodermatitis enteropathica Acrogeria, Gottron type Acrokeratoelastoidosis of Costa Actinic lichen planus Acute febrile neutrophilic dermatosis Acute intermittent porphyria Adams-Oliver syndrome Adiposis dolorosa ADULT syndrome Adult T-cell leukemia/lymphoma Ainhum Albinism deafness syndrome Al-Gazali-Donnai-Mueller syndrome Alkaptonuria Alopecia-contractures-dwarfism-intellectual disability syndrome Alopecia epilepsy oligophrenia syndrome of Moynahan Alopecia, epilepsy, pyorrhea, mental subnormality Alopecia-intellectual disability syndrome Alopecia totalis Alopecia universalis Ambras syndrome Ameloonychohypohidrotic syndrome Aminolevulinate dehydratase deficiency porphyria Amyopathic dermatomyositis Angioma serpiginosum Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Annular atrophic lichen planus Annular lichen planus Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges Antecubital pterygium Aplasia cutis congenita Aplasia cutis congenita intestinal lymphangiectasia Aplasia cutis congenita of limbs recessive AREDYLD Arterial tortuosity syndrome Arthrochalasia Ehlers-Danlos syndrome Arthrogryposis and ectodermal dysplasia Arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay Arthrogryposis renal dysfunction cholestasis syndrome Ataxia telangiectasia Atrophic lichen planus Atrophoderma of Pierini and Pasini Atrophoderma vermiculata Autoimmune hepatitis Autoimmune progesterone dermatitis Autosomal dominant deafness-onychodystrophy syndrome Autosomal dominant hyper IgE syndrome Autosomal dominant palmoplantar keratoderma and congenital alopecia Autosomal recessive candidiasis familial chronic mucocutaneous Autosomal recessive palmoplantar keratoderma and congenital alopecia

B Diseases

Bannayan-Riley-Ruvalcaba syndrome Barber Say syndrome Barraquer-Simons syndrome Basaran Yilmaz syndrome Bazex-Dupre-Christol syndrome Beare-Stevenson cutis gyrata syndrome Becker nevus syndrome Becker's nevus Behçet disease Benign eccrine spiradenoma Biotinidase deficiency Birt-Hogg-Dube syndrome Bjornstad syndrome Blau syndrome Blepharo-cheilo-odontic syndrome Bloom syndrome Blue rubber bleb nevus syndrome Book syndrome Bork Stender Schmidt syndrome Brittle cornea syndrome Brunsting-Perry syndrome Bullous dystrophy hereditary macular type Buschke Ollendorff syndrome

C Diseases

Campomelia Cumming type Cantu syndrome Cardiac-Valvular Ehlers-Danlos syndrome Cardiofaciocutaneous syndrome Cardiomyopathy dilated with woolly hair and keratoderma Carney complex Cartilage-hair hypoplasia Cerebellar ataxia ectodermal dysplasia Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Cerebro-oculo-facio-skeletal syndrome Cerebrotendinous xanthomatosis Cervical hypertrichosis peripheral neuropathy Chanarin-Dorfman syndrome Chediak-Higashi syndrome Cheilitis glandularis CHILD syndrome Chorea-acanthocytosis Chromhidrosis Chromosome 17q11.2 deletion syndrome