DermaMeth : Human DNA Methylation database for genes associated with dermatological disorders

Disease Gene Interaction Network

  • Acrodermatitis enteropathica
  • Alagille Syndrome
  • Albright's hereditary osteodystrophy
  • Alkaptonuria
  • Angioma serpiginosum, X-linked
  • Ataxia Telangiectasia
  • ATAXIA-TELANGIECTASIA-LIKE DISORDER 1
  • Basal Cell Nevus Syndrome
  • Bazex-Dupre-Christol syndrome
  • Blau syndrome
  • Bloom Syndrome
  • Buschke-Ollendorff syndrome
  • Calcinosis
  • Cardiofaciocutaneous syndrome
  • Carney Complex
  • Chondrodysplasia punctata 2, X-linked dominant
  • Chondrodysplasia punctata, brachytelephalangic
  • Chondrodysplasia Punctata, Rhizomelic
  • Chronic Granulomatous Disease
  • Cockayne Syndrome
  • Coproporphyria, Hereditary
  • Costello Syndrome
  • Cowden-Like Syndrome
  • Crouzon Syndrome With Acanthosis Nigricans
  • Cutis Gyrata Syndrome of Beare And Stevenson
  • Cutis Laxa
  • Cutis marmorata telangiectatica congenita
  • Darier Disease
  • Dermatomyositis
  • Dowling-Degos Disease
  • Down Syndrome
  • Dupuytren Contracture
  • Dysautonomia, Familial
  • Dyskeratosis Congenita
  • Epidermal Nevus
  • Epidermolysis Bullosa Dystrophica
  • Epidermolysis Bullosa Simplex
  • Erythema
  • Erythrokeratodermia Variabilis
  • Erythromelalgia
  • Fanconi Syndrome
  • Focal Dermal Hypoplasia
  • Fucosidosis
  • Gangliosidosis, GM1
  • Gaucher Disease
  • Gaucher Disease, Perinatal Lethal
  • Gaucher Disease, Type Iiic
  • Granulomatous Disease, Chronic
  • Granulomatous Disease, Chronic, X-Linked
  • Hallermann's Syndrome
  • Harlequin type ichthyosis
  • Hartnup Disease
  • Hay-Wells syndrome
  • Hemochromatosis
  • Hemochromatosis, type 2
  • Hemochromatosis, Type 2B
  • Hemochromatosis, type 3
  • Hemochromatosis, type 4
  • Hereditary Sensory And Autonomic Neuropathy
  • Hermansky Pudlak syndrome 2
  • Hidradenitis Suppurativa
  • Hyalinosis, Systemic
  • Hyperlipidemias
  • Ichthyosis
  • Ichthyosis Bullosa of Siemens
  • Ichthyosis Vulgaris
  • Ichthyosis, Lamellar
  • Ichthyosis, Lamellar, 5
  • Incontinentia Pigmenti
  • Job Syndrome
  • Johanson Blizzard syndrome
  • Keratosis Follicularis Spinulosa Decalvans
  • Klippel-Trenaunay-Weber Syndrome
  • Lamellar ichthyosis, type 2
  • Lamellar ichthyosis, type 3
  • LEOPARD Syndrome
  • Lipoid Proteinosis of Urbach and Wiethe
  • Lymphedema, Hereditary, IB
  • LYMPHEDEMA, HEREDITARY, IC
  • Lymphedema, Hereditary, II
  • Marfan Syndrome
  • Melkersson-Rosenthal Syndrome
  • MERRF Syndrome
  • Methylmalonic acidemia
  • MUCKLE-WELLS SYNDROME
  • Muir-Torre Syndrome
  • Myotonic Dystrophy
  • NA
  • Netherton Syndrome
  • Noonan Syndrome
  • Noonan Syndrome 2
  • Noonan syndrome 3
  • Noonan Syndrome 4
  • Noonan Syndrome 5
  • Noonan Syndrome 6
  • NOONAN SYNDROME 7
  • NOONAN SYNDROME-LIKE DISORDER
  • NOONAN SYNDROME-LIKE DISORDERHAIR
  • Oculocutaneous albinism type 2
  • Osseous Heteroplasia, Progressive
  • Pachyonychia Congenita
  • Piebaldism
  • Pilomatrixoma
  • Pityriasis Rubra Pilaris
  • Popliteal Pterygium Syndrome
  • Porphyria Cutanea Tarda
  • Porphyria, Acute Hepatic
  • Porphyria, Acute Intermittent
  • Porphyria, Erythropoietic
  • Porphyria, South African type
  • Porphyrias
  • Porphyrias, Hepatic
  • Port-Wine Stain
  • Prader-Willi Syndrome
  • Proteus Syndrome
  • Protoporphyria, Erythropoietic
  • PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED
  • Pseudoxanthoma Elasticum
  • Refsum Disease
  • Rothmund-Thomson Syndrome
  • Schimke immunoosseous dysplasia
  • Smith-Lemli-Opitz Syndrome
  • Steatocystoma Multiplex
  • Sturge-Weber Syndrome
  • Transient bullous dermolysis of the newborn
  • Trichothiodystrophy Syndromes
  • Tuberous Sclerosis
  • Tuberous Sclerosis 1
  • Tuberous Sclerosis 2
  • Tumoral Calcinosis, Hyperphosphatemic, Familial
  • Tumoral Calcinosis, Normophosphatemic, Familial
  • Turner Syndrome
  • Tyrosine Kinase 2 Deficiency
  • Vitiligo
  • WATSON SYNDROME
  • Werner Syndrome
  • Wiskott-Aldrich Syndrome
  • Xanthomatosis, Cerebrotendinous
  • Xeroderma Pigmentosum

Department of Biotechnology,
Delhi Technological University,Shahbad Daulatpur, Main Bawana Road, Delhi 110042
Email- yashahasija@dtu.ac.in; yashahaisja@gmail.com; raoshiva10@gmail.com