Fragile skin

Symptom Information:

Symptom ID: HPO:0001030
Synonyms:
Skin fragility [HPO:0001030]
Fragile skin [OMIM:Fragile skin]
Skin fragility [OMIM:Skin fragility]
Skin fragility [MedDRA:10040851]
Skin fragility of [MedDRA:10040851]
Dermatorrhexis [MedDRA:10040851]
Quality:
Cross references:
OMIM: "Fragile skin" [OMIM:Fragile skin]
OMIM: "Skin fragility" [OMIM:Skin fragility]
Is a (Direct Parents):
HPO         Generalized abnormality of skin
MedDRA Dermal and epidermal conditions NEC
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)
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)