Disease Browser
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Parent Node: Neoplasms by Site (D009371) |
Parent Node: Skin Diseases (D012871) |
..Starting node ..Skin Neoplasms (D012878)
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Child Nodes:
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........Abdominal chemodectomas with cutaneous angiolipomas (C535552) |
........Acanthoma (D049309) |
........Bazex-Dupre-Christol syndrome (C537663) |
........Becker Nevus Syndrome (C565735) |
........Blue rubber bleb nevus syndrome (C536240) |
........Calcifying Epithelial Odontogenic Tumor (C537961) |
........Cardiomyopathy hypogonadism collagenoma syndrome (C535582) |
........Collagenoma, Familial Cutaneous (C562925) |
........Davenport Donlan syndrome (C535988) |
........Dermatopathia pigmentosa reticularis (C535374) |
........Familial cylindromatosis (C536611) |
........Familial multiple trichodiscomas (C536847) |
........Fanconi like syndrome (C536855) |
........Giant pigmented hairy nevus (C536819) |
........Hamartoma, Precalcaneal Congenital Fibrolipomatous (C565226) |
........Histiocytosis, Progressive Mucinous (C564186) |
........MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 (OMIM:155600) |
........MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 (OMIM:155601) |
........MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 (OMIM:609048) |
........MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4 (OMIM:608035) |
........MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 (OMIM:613099) |
........MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7 (OMIM:612263) |
........MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 (OMIM:614456) |
........Nevus, Epidermal (C562736) |
........PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL (OMIM:610644) |
........Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal (C565693) |
........Papillomatosis, Familial Cutaneous (C566832) |
........Phacomatosis pigmentokeratotica (C537893) |
........Reactive angioendotheliomatosis (C535293) |
........Reed's syndrome (C535516) |
........Rombo syndrome (C535870) |
........Schwannomatosis (C536641) |
........Sclerotylosis (C537526) |
........Sebaceous Gland Neoplasms (D012626) 2 |
........Sweat Gland Neoplasms (D013544) |
........Trichoepithelioma, Multiple Familial, 2 (C567418) |
........Trichoepitheliomas, Multiple Desmoplastic (C566034) |
........Trichofolliculoma (C536553) |
........Tufted angioma (C536924) |
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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