Hyperextensible skin

Symptom Information:

Symptom ID: HPO:0000974
Synonyms:
Hyperelastic skin [HPO:0000974]
Skin hyperelasticity [HPO:0000974]
Skin hyperextensibility [HPO:0000974]
Stretchable skin [HPO:0000974]
Hyperelastic skin [OMIM:Hyperelastic skin]
Hyperextensible skin [OMIM:Hyperextensible skin]
Skin hyperelasticity [OMIM:Skin hyperelasticity]
Skin hyperextensibility [OMIM:Skin hyperextensibility]
Stretchable skin [OMIM:Stretchable skin]
Hyperelastic skin/cutaneous hyperlaxity [Orphanet:23460]
Hyperextensible skin (in some patients) [OMIM:Hyperextensible skin (in some patients)]
Skin hyperextensibility (rare) [OMIM:Skin hyperextensibility (rare)]
Quality:
Cross references:
HPO:0000973 "Cutis laxa" [Orphanet:23460]
HPO:0008067 "Abnormally lax or hyperextensible skin" [Orphanet:23460]
Orphanet:23460 "Hyperelastic skin/cutaneous hyperlaxity" [Orphanet:23460]
OMIM: "Hyperelastic skin" [OMIM:Hyperelastic skin]
OMIM: "Hyperextensible skin" [OMIM:Hyperextensible skin]
OMIM: "Skin hyperelasticity" [OMIM:Skin hyperelasticity]
OMIM: "Skin hyperextensibility" [OMIM:Skin hyperextensibility]
OMIM: "Stretchable skin" [OMIM:Stretchable skin]
OMIM: "Hyperextensible skin (in some patients)" [OMIM:Hyperextensible skin (in some patients)]
OMIM: "Skin hyperextensibility (rare)" [OMIM:Skin hyperextensibility (rare)]
Is a (Direct Parents):
Orphanet Abnormality of the skin
HPO         Abnormally lax or hyperextensible skin
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)
                   Abnormal elasticity of skin(HPO:0010647)
                      Abnormally lax or hyperextensible skin(HPO:0008067)
                         Hyperextensible skin(HPO:0000974)
MedDRA:
Database Frequency: 59 / 7739
Resource:

All diseases associated with this symptom:

AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
ALDH18A1-related De Barsy syndrome (Orphanet:35664)
Aarskog-Scott syndrome (Orphanet:915)
Arachnodactyly - abnormal ossification - intellectual deficit (Orphanet:1129)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Barber-Say syndrome (Orphanet:1231)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
Cardiofaciocutaneous syndrome (Orphanet:1340)
De Barsy syndrome (Orphanet:2962)
Diastrophic dwarfism (Orphanet:628)
EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED (OMIM:130090)
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE (OMIM:608763)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2 (OMIM:615349)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Ehlers-Danlos syndrome type 7A (Orphanet:99875)
Ehlers-Danlos syndrome type 7B (Orphanet:99876)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
Ehlers-Danlos syndrome, cardiac valvular type (Orphanet:230851)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, fibronectinemic type (Orphanet:75501)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type (Orphanet:300179)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Ehlers-Danlos syndrome, periodontitis type (Orphanet:75392)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
Eyebrow duplication - syndactyly (Orphanet:3172)
FIBRINOLYTIC DEFECT (OMIM:134900)
Fountain syndrome (Orphanet:3219)
GAPO syndrome (Orphanet:2067)
Geroderma osteodysplastica (Orphanet:2078)
Granulomatous slack skin (Orphanet:33111)
LOEYS-DIETZ SYNDROME, TYPE 2A (OMIM:608967)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Lysinuric protein intolerance (Orphanet:470)
MACS syndrome (Orphanet:217335)
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2 (OMIM:615937)
Marden-Walker syndrome (Orphanet:2461)
Marfan syndrome type 2 (Orphanet:284973)
Marshall-Smith syndrome (Orphanet:561)
Menkes disease (Orphanet:565)
NOONAN SYNDROME 8 (OMIM:615355)
Noonan syndrome with multiple lentigines (Orphanet:500)
Occipital horn syndrome (Orphanet:198)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Pseudoxanthoma elasticum (Orphanet:758)
Renal coloboma syndrome (Orphanet:1475)
SCARF syndrome (Orphanet:3134)
Sakati-Nyhan syndrome (Orphanet:3128)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Spinocerebellar ataxia - dysmorphism (Orphanet:1185)
Spondylo-ocular syndrome (Orphanet:85194)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
X-linked Ehlers-Danlos syndrome (Orphanet:75497)