Facial erythema
Symptom Information:
Symptom ID: | HPO:0001041 | ||
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) Vascular skin abnormality(HPO:0011276) Erythema(HPO:0010783) Facial erythema(HPO:0001041) 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) |
Cushing disease | (Orphanet:96253) |
DERMATITIS, ATOPIC | (OMIM:603165) |
DERMODISTORTIVE URTICARIA | (OMIM:125630) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT | (OMIM:612843) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED | (OMIM:308800) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE | (OMIM:143850) |