Sclerodactyly
Symptom Information:
Symptom ID: | HPO:0011838 | ||
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) Sclerodactyly(HPO:0011838) MedDRA: |
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Database Frequency: | 8 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive palmoplantar keratoderma and congenital alopecia | (Orphanet:1366) |
CREST syndrome | (Orphanet:90290) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Limited systemic sclerosis | (Orphanet:220407) |
Pediatric systemic sclerosis | (Orphanet:93567) |
Reynolds syndrome | (Orphanet:779) |
Systemic sclerosis | (Orphanet:90291) |