Disease Browser
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Parent Node: Keratoderma, Palmoplantar (D007645) |
..Starting node ..Keratoderma, Palmoplantar, Norrbotten Recessive Type (C565454)
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Child Nodes:
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Sister Nodes: |
..Acrokeratoelastoidosis of Costa (C535653)
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..Alopecia congenita keratosis palmoplantaris (C537050)
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..Basaran Yilmaz syndrome (C537660)
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..Cardiomyopathy dilated with Woolly hair and keratoderma (C535581)
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..Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome (C537943)
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..Corneodermatoosseous syndrome (C536444)
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..Fitzsimmons-McLachlan-Gilbert syndrome (C537058)
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..Hyperkeratosis-Hyperpigmentation Syndrome (C564172)
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..Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome (C564357)
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..Judge Misch Wright syndrome (C537692)
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..Keratoderma palmoplantar deafness (C536152)
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..Keratoderma palmoplantar spastic paralysis (C536153)
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..Keratoderma, Palmoplantar, Diffuse (D015776) 7
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..Keratoderma, Palmoplantar, Norrbotten Recessive Type (C565454)
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..Keratosis focal palmoplantar gingival (C536157)
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..Keratosis Palmaris et Plantaris with Clinodactyly (C563646)
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..Keratosis palmoplantaris papulosa (C536161)
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..Keratosis palmoplantaris striata 1 (C536162)
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..Keratosis palmoplantaris striata 3 (C536163)
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..Keratosis Palmoplantaris Striata II (C565102)
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..Keratosis palmoplantaris with esophageal cancer (C536164)
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..Knuckle pads, leuconychia and sensorineural deafness (C537210)
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..Naegeli syndrome (C538331)
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..Naxos disease (C538346)
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..Palmoplantar Hyperkeratosis And True Hermaphroditism (C567165)
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..PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL (OMIM:610644)
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..Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal (C565693)
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..Palmoplantar Keratoderma with Deafness (C580359)
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..Palmoplantar Keratoderma, Epidermolytic, with Knuckle Pads (C564171)
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..Papillon-Lefevre Disease (D010214) 2
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..Patel Bixler syndrome (C536306)
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..Porokeratosis punctata palmaris et plantaris (C536338)
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..Powell Venencie Gordon syndrome (C538358)
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..Schopf-Schulz-Passarge Syndrome (C565607)
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..Stern Lubinsky Durrie syndrome (C537488)
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..Vohwinkel syndrome (C536457)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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