Diffuse palmoplantar hyperkeratosis
Symptom Information:
Symptom ID: | HPO:0007447 | ||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Abnormality of the palm(HPO:0100871) Palmoplantar hyperkeratosis(HPO:0000972) Diffuse palmoplantar hyperkeratosis(HPO:0007447) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Regional abnormality of skin(HPO:0011356) Abnormality of the plantar skin of foot(HPO:0100872) Palmoplantar hyperkeratosis(HPO:0000972) Diffuse palmoplantar hyperkeratosis(HPO:0007447) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Thickened skin(HPO:0001072) Epidermal thickening(HPO:0011368) Hyperkeratosis(HPO:0000962) Palmar hyperkeratosis(HPO:0010765) Palmoplantar hyperkeratosis(HPO:0000972) Diffuse palmoplantar hyperkeratosis(HPO:0007447) Plantar hyperkeratosis(HPO:0007556) Palmoplantar hyperkeratosis(HPO:0000972) Diffuse palmoplantar hyperkeratosis(HPO:0007447) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cornification and dystrophic skin disorders(MedDRA:10011063) Hyperkeratoses(MedDRA:10020648) Diffuse palmoplantar hyperkeratosis(HPO:0007447) |
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Database Frequency: | 8 / 7739 | ||||||||||||||
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All diseases associated with this symptom:
Arrhythmogenic right ventricular dysplasia, familial, 11 | (OMIM:610476) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
Epidermolytic palmoplantar keratoderma | (Orphanet:2199) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 | (OMIM:604777) |
Keratosis palmaris et plantaris - clinodactyly | (Orphanet:86919) |
Palmoplantar keratoderma-esophageal carcinoma syndrome | (Orphanet:2198) |
Tyrosinemia type 2 | (Orphanet:28378) |