Palmoplantar keratoderma
Symptom Information:
Symptom ID: | HPO:0000982 | |||||||||||||||
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 integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Thickened skin(HPO:0001072) Epidermal thickening(HPO:0011368) Hyperkeratosis(HPO:0000962) Palmoplantar keratoderma(HPO:0000982) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cornification and dystrophic skin disorders(MedDRA:10011063) Hyperkeratoses(MedDRA:10020648) Palmoplantar keratoderma(HPO:0000982) |
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Database Frequency: | 40 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Arrhythmogenic right ventricular dysplasia, familial, 11 | (OMIM:610476) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
CEDNIK syndrome | (Orphanet:66631) |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | (OMIM:615821) |
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis | (Orphanet:352662) |
Diffuse palmoplantar keratoderma with painful fissures | (Orphanet:369999) |
Ectodermal dysplasia - cutaneous syndactyly syndrome | (Orphanet:247827) |
Epidermolytic palmoplantar keratoderma | (Orphanet:2199) |
Exfoliative ichthyosis | (Orphanet:289586) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Hereditary palmoplantar keratoderma, Gamborg-Nielsen type | (Orphanet:86923) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10 | (OMIM:615024) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A | (OMIM:601277) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 | (OMIM:604777) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 | (OMIM:612281) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7 | (OMIM:615022) |
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS | (OMIM:602540) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED | (OMIM:308800) |
KERATOSIS PALMOPLANTARIS STRIATA II | (OMIM:612908) |
KERATOSIS PALMOPLANTARIS STRIATA III | (OMIM:607654) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Keratosis palmaris et plantaris - clinodactyly | (Orphanet:86919) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
Naegeli-Franceschetti-Jadassohn syndrome | (Orphanet:69087) |
Naxos disease | (Orphanet:34217) |
PACHYONYCHIA CONGENITA 3 | (OMIM:615726) |
PACHYONYCHIA CONGENITA 4 | (OMIM:615728) |
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR | (OMIM:616099) |
PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES, X-LINKED | (OMIM:300918) |
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL | (OMIM:613000) |
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE | (OMIM:615735) |
PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS,AND KNUCKLE PADS | (OMIM:616295) |
Palmoplantar keratoderma-spastic paralysis syndrome | (Orphanet:2201) |
Pityriasis rubra pilaris | (Orphanet:2897) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Self-healing collodion baby | (Orphanet:281122) |
Tyrosinemia type 2 | (Orphanet:28378) |
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | (Orphanet:65282) |
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 | (OMIM:107970) |