Parakeratosis
Symptom Information:
Symptom ID: | HPO:0001036 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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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) Parakeratosis(HPO:0001036) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Dermal and epidermal conditions NEC(MedDRA:10012424) Parakeratosis(HPO:0001036) |
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Database Frequency: | 12 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
CHILD syndrome | (Orphanet:139) |
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis | (Orphanet:352662) |
Generalized pustular psoriasis | (Orphanet:247353) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 | (OMIM:604777) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 | (OMIM:612281) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
Keratoderma hereditarium mutilans with ichthyosis | (Orphanet:79395) |
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome | (Orphanet:281201) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES, X-LINKED | (OMIM:300918) |
PSORIASIS 2 | (OMIM:602723) |
Palmoplantar keratoderma-esophageal carcinoma syndrome | (Orphanet:2198) |