Ontomatica – ChEMATIC (Wedge)

The current query selects 3456 items in 73 groups, which could be too many to show at once. If you are sure you want to see them all, you can proceed to see the entire category, 'or select a more specific subcategory of "Skin Diseases, Genetic [MESH:D012873]" below.

Subcategories in Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342] > Skin Diseases, Genetic [MESH:D012873]:
(jump to A - B - C - D - E - F - G - H - I - J - K - L - M - N - O - P - R - S - T - V - X)

- A -
Actinic Prurigo [MESH:C566780] (1)
Albinism [MESH:D000417] (359)
Amyloidosis IX [MESH:C562643] (52)
Amyloidosis, Cutaneous Bullous [MESH:C562644] (1)
Amyloidosis, Primary Cutaneous [MESH:C562642] (1)
Annular Erythema [MESH:C562461] (1)
Arterial Tortuosity Syndrome [MESH:C565942] (12)
Atrophia Maculosa Varioliformis Cutis, Familial [MESH:C563349] (1)

- B -
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant [MESH:C565284] (1)
Buschke-Ollendorff syndrome [MESH:C537415] (11)

- C -
Collagenosis, Familial Reactive Perforating [MESH:C565687] (1)
Cutis Laxa [MESH:D003483] (177)

- D -
Darier Disease [MESH:D007644] (125)
Dermatitis, Atopic [MESH:D003876] (2052)
Dyschromatosis Universalis Hereditaria 1 [MESH:C567273] (1)
Dyschromatosis Universalis Hereditaria 2 [MESH:C567194] (1)
Dyschromatosis universalis hereditaria [MESH:C535730] (1)
Dyskeratosis Congenita [MESH:D019871] (185)
dowling-degos disease [MESH:C562924] (53)

- E -
Ectodermal Dysplasia [MESH:D004476] (958)
Ehlers-Danlos Syndrome [MESH:D004535] (491)
Epidermolysis Bullosa [MESH:D004820] (259)
Erythrokeratodermia Variabilis [MESH:D056266] (26)
Erythrokeratodermia with ataxia [MESH:C535738] (1)
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like [MESH:C564309] (1)

- F -
Fingerprints, Absence of [MESH:C565010] (1)
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts [MESH:C566360] (1)

- G -
Gerodermia osteodysplastica [MESH:C537799] (12)

- H -
Histiocytic Dermatoarthritis [MESH:C564183] (1)
Hyalinosis, Systemic [MESH:D057770] (24)
Hyaluronan Metabolism, Defect in [MESH:C565742] (1)

- I -
Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)
Ichthyosis Bullosa of Siemens [MESH:D053560] (14)
Ichthyosis Vulgaris [MESH:D016112] (27)
Ichthyosis, X-Linked [MESH:D016114] (91)
Incontinentia Pigmenti [MESH:D007184] (57)

- J -
Juvenile Spring Eruption of Ears [MESH:C566781] (1)

- K -
Keratoderma, Palmoplantar [MESH:D007645] (287)
Keratolytic winter erythema [MESH:C536155] (1)
Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma [MESH:C566600] (15)

- L -
Leukokeratosis, Hereditary Mucosal [MESH:D053529] (51)
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis [MESH:C565440] (1)
Lipoid Proteinosis of Urbach and Wiethe [MESH:D008065] (38)

- M -
Monilethrix [MESH:D056734] (17)

- N -
Netherton Syndrome [MESH:D056770] (43)
Noduli Cutanei, Multiple, with Urinary Tract Abnormalities [MESH:C563512] (1)

- O -
Oculotrichodysplasia [MESH:C564934] (1)
Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair [MESH:C563506] (1)
Orofaciodigital syndrome 9 [MESH:C557818] (1)
Osseous Heteroplasia, Progressive [MESH:C562735] (82)
Osteopoikilosis, Isolated [MESH:C563484] (1)

- P -
Parana Hard Skin Syndrome [MESH:C564905] (1)
Peeling Skin Syndrome [MESH:C564818] (9)
Pemphigus, Benign Familial [MESH:D016506] (22)
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial [MESH:C562486] (1)
Pigmentary Disorder, Reticulate, with Systemic Manifestations [MESH:C564461] (1)
Plasminogen Deficiency, Type I [MESH:C566897] (83)
Poikiloderma, Hereditary Sclerosing [MESH:C562824] (1)
Porokeratosis [MESH:D017499] (59)
Porphyria, Erythropoietic [MESH:D017092] (16)
Porphyrias, Hepatic [MESH:D017094] (881)
Prolidase Deficiency [MESH:D056732] (46)
Pseudoxanthoma Elasticum [MESH:D011561] (115)

- R -
Rothmund-Thomson Syndrome [MESH:D011038] (35)

- S -
Sjogren-Larsson Syndrome [MESH:D016111] (67)
Skin Fragility-Woolly Hair Syndrome [MESH:C564359] (37)
Stiff Skin Syndrome [MESH:C566112] (62)
Storm Syndrome [MESH:C566109] (1)

- T -
Trichothiodystrophy Syndromes [MESH:D054463] (5)

- V -
Vitiligo, Progressive, with Mental Retardation and Urethral Duplication [MESH:C564739] (1)
Vohwinkel Syndrome, Variant Form [MESH:C565826] (22)

- X -
Xeroderma Pigmentosum [MESH:D014983] (213)