Porokeratosis
Symptom Information:
Symptom ID: | HPO:0200044 | ||||
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) Porokeratosis(HPO:0200044) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Skin and subcutaneous tissue disorders congenital(MedDRA:10040789) Skin and subcutaneous tissue disorders congenital NEC(MedDRA:10040834) Porokeratosis(HPO:0200044) |
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Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
AL amyloidosis | (Orphanet:85443) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
Disseminated superficial actinic porokeratosis | (Orphanet:79152) |
POROKERATOSIS 3, DISSEMINATED SUPERFICIAL ACTINIC TYPE | (OMIM:175900) |
POROKERATOSIS 6, DISSEMINATED SUPERFICIAL ACTINIC TYPE | (OMIM:612353) |
POROKERATOSIS 7, DISSEMINATED SUPERFICIAL ACTINIC TYPE | (OMIM:614714) |
POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE | (OMIM:616063) |
Porokeratosis of Mibelli | (Orphanet:735) |
Porokeratosis plantaris palmaris et disseminata | (Orphanet:737) |
Primary localized amyloidosis | (Orphanet:314709) |
Punctate palmoplantar keratoderma type 2 | (Orphanet:79502) |