| Disease Browser
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Parent Node:
 Osteopoikilosis (D010023) |
Parent Node:
Skin Diseases, Genetic (D012873) |
..Starting node
.. Osteopoikilosis, Isolated (C563484)
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Child Nodes:
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Sister Nodes: |
..Actinic Prurigo (C566780)
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..Albinism (D000417)  30
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..Amyloidosis IX (C562643)
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..Amyloidosis, Cutaneous Bullous (C562644)
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..Amyloidosis, Primary Cutaneous (C562642)
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..Annular Erythema (C562461)
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..Arterial Tortuosity Syndrome (C565942)
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..Atrophia Maculosa Varioliformis Cutis, Familial (C563349)
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..Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant (C565284)
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..Buschke-Ollendorff syndrome (C537415)
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..Collagenosis, Familial Reactive Perforating (C565687)
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..Cutis Laxa (D003483) 17
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..Darier Disease (D007644) 7
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..Dermatitis, Atopic (D003876) 9
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..dowling-degos disease (C562924)
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..Dyschromatosis universalis hereditaria (C535730)
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..Dyschromatosis Universalis Hereditaria 1 (C567273)
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..Dyschromatosis Universalis Hereditaria 2 (C567194)
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..Dyskeratosis Congenita (D019871) 3
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..Ectodermal Dysplasia (D004476) 144
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..Ehlers-Danlos Syndrome (D004535) 23
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..Epidermolysis Bullosa (D004820) 29
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..Erythrokeratodermia Variabilis (D056266) 3
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..Erythrokeratodermia with ataxia (C535738)
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..Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like (C564309)
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..Fingerprints, Absence of (C565010)
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..Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts (C566360)
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..Gerodermia osteodysplastica (C537799)
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..Hereditary Autoinflammatory Diseases (D056660) 10
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..Histiocytic Dermatoarthritis (C564183)
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..Hyalinosis, Systemic (D057770)
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..Hyaluronan Metabolism, Defect in (C565742)
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..Ichthyosiform Erythroderma, Congenital (D016113) 18
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..Ichthyosis Bullosa of Siemens (D053560)
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..Ichthyosis Vulgaris (D016112) 1
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..Ichthyosis, X-Linked (D016114) 2
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..Incontinentia Pigmenti (D007184) 2
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..Juvenile Spring Eruption of Ears (C566781)
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..Keratoderma, Palmoplantar (D007645) 45
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..Keratolytic winter erythema (C536155)
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..Keratosis Follicularis Spinulosa Decalvans, X-Linked (C536159)
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..Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma (C566600)
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..Leukokeratosis, Hereditary Mucosal (D053529)
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..Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis (C565440)
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..Lipoid Proteinosis of Urbach and Wiethe (D008065)
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..Monilethrix (D056734) 1
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..Muir-Torre Syndrome (D055653)
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..Netherton Syndrome (D056770)
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..Noduli Cutanei, Multiple, with Urinary Tract Abnormalities (C563512)
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..Oculotrichodysplasia (C564934)
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..Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair (C563506)
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..Orofaciodigital syndrome 9 (C557818)
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..Osseous Heteroplasia, Progressive (C562735)
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..Osteopoikilosis, Isolated (C563484)
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..Parana Hard Skin Syndrome (C564905)
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..Peeling Skin Syndrome (C564818)
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..Pemphigus, Benign Familial (D016506)
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..Perifolliculitis Capitis Abscedens Et Suffodiens, Familial (C562486)
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..Pigmentary Disorder, Reticulate, with Systemic Manifestations (C564461)
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..Plasminogen Deficiency, Type I (C566897)
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..Poikiloderma, Hereditary Sclerosing (C562824)
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..Porokeratosis (D017499) 7
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..Porphyria, Erythropoietic (D017092)
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..Porphyrias, Hepatic (D017094) 14
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..Prolidase Deficiency (D056732)
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..Pseudoxanthoma Elasticum (D011561) 2
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..Rothmund-Thomson Syndrome (D011038) 5
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..Sjogren-Larsson Syndrome (D016111) 1
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..Skin Fragility-Woolly Hair Syndrome (C564359)
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..Stiff Skin Syndrome (C566112)
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..Storm Syndrome (C566109)
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..Trichothiodystrophy Syndromes (D054463) 5
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..Vitiligo, Progressive, with Mental Retardation and Urethral Duplication (C564739)
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..Vohwinkel Syndrome, Variant Form (C565826)
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..Xeroderma Pigmentosum (D014983) 16
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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