Ontomatica – ChEMATIC (Wedge)

The current query selects 1709 items in 55 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 Abnormalities [MESH:D012868]" below.

Subcategories in Skin Diseases [MESH:D012871] > Skin Abnormalities [MESH:D012868]:
(jump to A - B - C - D - E - F - H - I - K - M - O - P - R - S - T - U - V - W - X)

- A -
Acrodermatitis [MESH:D000169] (56)
Anetoderma [MESH:D057088] (3)
Arthropathy, Erosive [MESH:C565273] (1)

- B -
Barber Say syndrome [MESH:C537908] (1)
Blepharophimosis syndrome type 1 [MESH:C536233] (12)
Blepharophimosis syndrome type 2 [MESH:C536234] (1)
Blepharophimosis with ptosis, syndactyly, and short stature [MESH:C536235] (1)
Blepharophimosis, Ptosis, and Epicanthus Inversus [MESH:C562419] (12)
Book Syndrome [MESH:C562993] (1)

- C -
Comedones, Familial Dyskeratotic [MESH:C562838] (1)
Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)

- D -
Dermal Ridges, Nelson Syndrome [MESH:C565110] (1)
Dermal Ridges, Patternless [MESH:C565109] (1)
Dermoodontodysplasia [MESH:C565103] (1)
Dyskeratosis Congenita [MESH:D019871] (185)
Dyskeratosis, Hereditary Benign Intraepithelial [MESH:C562551] (1)

- E -
Ectodermal Dysplasia [MESH:D004476] (958)
Ehlers-Danlos Syndrome [MESH:D004535] (491)
Epidermolysis Bullosa [MESH:D004820] (260)
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract [MESH:C565584] (1)

- F -
Familial popliteal pterygium syndrome [MESH:C535891] (1)

- H -
Hairy palms and soles [MESH:C535620] (1)
Hemangiomatosis, Cutaneous, with Associated Features [MESH:C562438] (1)
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations [MESH:C566153] (1)
Hypohidrosis aith Abnormal Palmar Dermal Ridges [MESH:C565481] (1)

- I -
Ichthyosis [MESH:D007057] (481)
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin [MESH:C563402] (1)
Incontinentia Pigmenti [MESH:D007184] (57)

- K -
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma [MESH:C566600] (15)

- M -
Michelin tire baby syndrome [MESH:C537575] (1)
Microphthalmia, syndromic 7 [MESH:C537466] (18)
Multiple pterygium syndrome [MESH:C537377] (23)

- O -
Oculocerebrocutaneous syndrome [MESH:C538088] (1)

- P -
Poikiloderma with Neutropenia [MESH:C565820] (4)
Poikiloderma, Hereditary Sclerosing [MESH:C562824] (1)
Port-Wine Stain [MESH:D019339] (86)
Pseudoxanthoma Elasticum [MESH:D011561] (115)
Pterygium Colli, Isolated [MESH:C566741] (1)

- R -
Ridges-off-the-end syndrome [MESH:C531754] (1)
Rothmund-Thomson Syndrome [MESH:D011038] (35)

- S -
Sclerema Neonatorum [MESH:D012593] (1)
Skin/Hair/Eye Pigmentation, Variation In, 10 [MESH:C567376] (1)
Skin/Hair/Eye Pigmentation, Variation In, 11 [MESH:C567374] (1)
Skin/Hair/Eye Pigmentation, Variation In, 4 [MESH:C567300] (1)
Skin/Hair/Eye Pigmentation, Variation In, 5 [MESH:C567119] (1)
Skin/Hair/Eye Pigmentation, Variation In, 6 [MESH:C567139] (1)
Skin/Hair/Eye Pigmentation, Variation In, 7 [MESH:C567155] (1)
Skin/Hair/Eye Pigmentation, Variation In, 8 [MESH:C567096] (1)
Skin/Hair/Eye Pigmentation, Variation In, 9 [MESH:C567091] (1)

- T -
Tight skin contracture syndrome, lethal [MESH:C536920] (84)
Trichothiodystrophy Syndromes [MESH:D054463] (5)

- U -
Urban Schosser Spohn syndrome [MESH:C536476] (1)

- V -
Vascular Hyalinosis [MESH:C564750] (1)

- W -
Winter Shortland Temple syndrome [MESH:C536735] (1)

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