Palmoplantar hyperkeratosis
Symptom Information:
Symptom ID: | HPO:0000972 | |||||||||||||||||||||||
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) 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) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Thickened skin(HPO:0001072) Epidermal thickening(HPO:0011368) Hyperkeratosis(HPO:0000962) Plantar hyperkeratosis(HPO:0007556) Palmoplantar hyperkeratosis(HPO:0000972) Palmar hyperkeratosis(HPO:0010765) Palmoplantar hyperkeratosis(HPO:0000972) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cornification and dystrophic skin disorders(MedDRA:10011063) Hyperkeratoses(MedDRA:10020648) Palmoplantar hyperkeratosis(HPO:0000972) |
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Database Frequency: | 41 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME | (OMIM:231550) |
ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS | (OMIM:206600) |
Annular epidermolytic ichthyosis | (Orphanet:281139) |
Arrhythmogenic right ventricular dysplasia, familial, 11 | (OMIM:610476) |
Autosomal dominant palmoplantar keratoderma and congenital alopecia | (Orphanet:1010) |
Autosomal recessive palmoplantar keratoderma and congenital alopecia | (Orphanet:1366) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Congenital reticular ichthyosiform erythroderma | (Orphanet:281190) |
Cowden syndrome | (Orphanet:201) |
Cranio-osteoarthropathy | (Orphanet:1525) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 | (OMIM:613989) |
Dermatopathia pigmentosa reticularis | (Orphanet:86920) |
EPIDERMOLYTIC HYPERKERATOSIS | (OMIM:113800) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Epidermolysis bullosa simplex, Dowling-Meara type | (Orphanet:79396) |
Epidermolytic ichthyosis | (Orphanet:312) |
Epidermolytic palmoplantar keratoderma | (Orphanet:2199) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type | (Orphanet:79399) |
Hereditary acrokeratotic poikiloderma of Kindler-Weary | (Orphanet:306539) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome | (Orphanet:363523) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 | (OMIM:604777) |
Keratosis palmaris et plantaris - clinodactyly | (Orphanet:86919) |
Lhermitte-Duclos disease | (Orphanet:65285) |
PACHYONYCHIA CONGENITA 1 | (OMIM:167200) |
PACHYONYCHIA CONGENITA 2 | (OMIM:167210) |
PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES, X-LINKED | (OMIM:300918) |
Pachyonychia congenita | (Orphanet:2309) |
Palmoplantar keratoderma-deafness syndrome | (Orphanet:2202) |
Papillon-Lefèvre syndrome | (Orphanet:678) |
Paraplegia - intellectual deficit - hyperkeratosis | (Orphanet:2824) |
Proteus-like syndrome | (Orphanet:2969) |
Rosselli-Gulienetti syndrome | (Orphanet:90339) |
Stern-Lubinsky-Durrie syndrome | (Orphanet:3194) |
Triple A syndrome | (Orphanet:869) |
Tyrosinemia type 2 | (Orphanet:28378) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |
Zunich-Kaye syndrome | (Orphanet:3474) |