Fragile skin
Symptom Information:
Symptom ID: | HPO:0001030 | ||||||
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) Fragile skin(HPO:0001030) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Dermal and epidermal conditions NEC(MedDRA:10012424) Fragile skin(HPO:0001030) |
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Database Frequency: | 25 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
AL amyloidosis | (Orphanet:85443) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Dystrophic epidermolysis bullosa pruriginosa | (Orphanet:89843) |
EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS | (OMIM:132000) |
EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE | (OMIM:615028) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
Epidermolysis bullosa simplex with pyloric atresia | (Orphanet:158684) |
Hepatoerythropoietic porphyria | (Orphanet:95159) |
Hereditary acrokeratotic poikiloderma of Kindler-Weary | (Orphanet:306539) |
Junctional epidermolysis bullosa - pyloric atresia | (Orphanet:79403) |
Naxos disease | (Orphanet:34217) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 | (OMIM:615830) |
Porphyria cutanea tarda | (Orphanet:101330) |
Primary systemic amyloidosis | (Orphanet:314701) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Skin fragility-woolly hair-palmoplantar keratoderma syndrome | (Orphanet:293165) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Transient bullous dermolysis of the newborn | (Orphanet:79411) |