| Disease Browser
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Parent Node:
 Congenital Abnormalities (D000013) |
Parent Node:
Skin Diseases (D012871) |
..Starting node
.. Skin Abnormalities (D012868)
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Child Nodes:
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........Acrodermatitis (D000169)  1 |
| ........Anetoderma (D057088) 2 |
| ........Arthropathy, Erosive (C565273) |
| ........Barber Say syndrome (C537908) |
| ........Blepharophimosis syndrome type 1 (C536233) |
| ........Blepharophimosis syndrome type 2 (C536234) |
| ........Blepharophimosis with ptosis, syndactyly, and short stature (C536235) |
| ........Blepharophimosis, Ptosis, and Epicanthus Inversus (C562419) |
| ........Book Syndrome (C562993) |
| ........Carney Complex (D056733) 1 |
| ........COCOON SYNDROME (OMIM:613630) |
| ........Comedones, Familial Dyskeratotic (C562838) |
| ........Cutis Gyrata Syndrome of Beare And Stevenson (C565129) |
| ........Dermal Ridges, Nelson Syndrome (C565110) |
| ........Dermal Ridges, Patternless (C565109) |
| ........Dermoodontodysplasia (C565103) |
| ........Dyskeratosis Congenita (D019871) 3 |
| ........Dyskeratosis, Hereditary Benign Intraepithelial (C562551) |
| ........Ectodermal Dysplasia (D004476) 144 |
| ........Ehlers-Danlos Syndrome (D004535) 23 |
| ........Epidermolysis Bullosa (D004820) 29 |
| ........Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract (C565584) |
| ........Familial popliteal pterygium syndrome (C535891) |
| ........Hairy palms and soles (C535620) |
| ........Hemangiomatosis, Cutaneous, with Associated Features (C562438) |
| ........Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations (C566153) |
| ........Hypohidrosis aith Abnormal Palmar Dermal Ridges (C565481) |
| ........Ichthyosis (D007057) 66 |
| ........Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin (C563402) |
| ........Incontinentia Pigmenti (D007184) 2 |
| ........Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma (C566600) |
| ........Michelin tire baby syndrome (C537575) |
| ........Microphthalmia, syndromic 7 (C537466) |
| ........Multiple pterygium syndrome (C537377) 1 |
| ........Oculocerebrocutaneous syndrome (C538088) |
| ........Poikiloderma with Neutropenia (C565820) |
| ........Poikiloderma, Hereditary Sclerosing (C562824) |
| ........Port-Wine Stain (D019339) 4 |
| ........Prolidase Deficiency (D056732) |
| ........Pseudoxanthoma Elasticum (D011561) 2 |
| ........Pterygium Colli, Isolated (C566741) |
| ........Ridges-off-the-end syndrome (C531754) |
| ........Rothmund-Thomson Syndrome (D011038) 5 |
| ........Sclerema Neonatorum (D012593) |
| ........Skin/Hair/Eye Pigmentation, Variation In, 10 (C567376) |
| ........Skin/Hair/Eye Pigmentation, Variation In, 11 (C567374) |
| ........Skin/Hair/Eye Pigmentation, Variation In, 4 (C567300) |
| ........Skin/Hair/Eye Pigmentation, Variation In, 5 (C567119) |
| ........Skin/Hair/Eye Pigmentation, Variation In, 6 (C567139) |
| ........Skin/Hair/Eye Pigmentation, Variation In, 7 (C567155) |
| ........Skin/Hair/Eye Pigmentation, Variation In, 8 (C567096) |
| ........Skin/Hair/Eye Pigmentation, Variation In, 9 (C567091) |
| ........Tight skin contracture syndrome, lethal (C536920) |
| ........Trichothiodystrophy Syndromes (D054463) 5 |
| ........Urban Schosser Spohn syndrome (C536476) |
| ........Vascular Hyalinosis (C564750) |
| ........Winter Shortland Temple syndrome (C536735) |
| ........Xeroderma Pigmentosum (D014983) 16 |
Sister Nodes: |
..Acneiform Eruptions (D017486) 5
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..Angiolymphoid Hyperplasia with Eosinophilia (D000796)
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..Borrone Di Rocco Crovato syndrome (C536577)
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..Boudhina Yedes Khiari syndrome (C537939)
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..Breast Diseases (D001941) 45
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..C SYNDROME (OMIM:211750)
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..Cutaneous Fistula (D017577)
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..Dermatitis (D003872) 57
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..Dermatoleukodystrophy (C538220)
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..Dermatomyositis (D003882) 2
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..Ectodermal dysplasia/ skin fragility syndrome (C536183)
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..Elastosis perforans serpiginosa (C536202)
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..Elliott Ludman Teebi syndrome (C536204)
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..Erythema (D004890) 19
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..Exanthema (D005076) 1
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..Eyebrows duplication of, with stretchable skin and syndactyly (C536383)
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..FACES syndrome (C536384)
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..Facial Dermatoses (D005148) 11
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..Facial ectodermal dysplasia (C536385)
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..Flynn Aird syndrome (C537066)
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..Foot Diseases (D005534) 13
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..Hair Diseases (D006201) 174
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..Hand Dermatoses (D006229) 1
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..Hernandez Fragoso syndrome (C536062)
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..Keratoacanthoma (D007636) 1
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..Keratosis (D007642) 149
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..Leg Dermatoses (D007868)
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..Lipomatosis (D008068) 11
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..Lupus Erythematosus, Cutaneous (D008178) 3
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..Macroepiphyseal dysplasia, McAlister Coe type (C537721)
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..MASS syndrome (C536030)
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..Mastocytosis (D008415) 9
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..Median cleft lip, corpus callosum, lipoma, and skin polyps (C536135)
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..Mental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities (C567209)
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..Morgellons Disease (D055535)
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..Nail Diseases (D009260) 42
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..Necrobiotic Disorders (D017441) 3
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..Necrolytic Migratory Erythema (D058568)
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..Nephrogenic Fibrosing Dermopathy (D054989)
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..OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS (OMIM:612852)
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..Panniculitis (D015434) 6
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..Photosensitivity Disorders (D010787) 31
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..Pigmentation Disorders (D010859) 147
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..Prurigo (D011536)
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..Pruritus (D011537) 6
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..Pseudoatrophoderma Colli (C562909)
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..Pyoderma (D011711) 3
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..Rosacea (D012393) 1
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..Roy Maroteaux Kremp syndrome (C535875)
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..Scalp Dermatoses (D012536) 10
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..Scleredema Adultorum (D012592)
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..Scleroderma, Localized (D012594) 5
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..Scleroderma, Systemic (D012595) 7
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..Sebaceous Gland Diseases (D012625) 12
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..Skin Abnormalities (D012868) 358
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..Skin Diseases, Eczematous (D017443) 35
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..Skin Diseases, Genetic (D012873) 462
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..Skin Diseases, Infectious (D012874) 103
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..Skin Diseases, Metabolic (D012875) 33
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..Skin Diseases, Papulosquamous (D017444) 26
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..Skin Diseases, Vascular (D017445) 33
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..Skin Diseases, Vesiculobullous (D012872) 54
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..Skin Neoplasms (D012878) 41
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..Skin Ulcer (D012883) 10
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..Sweat Gland Diseases (D013543) 25
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..Upton Young syndrome (C536473)
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..Xanthogranuloma, Juvenile (D014972)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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