Hyperextensible skin
Symptom Information:
Symptom ID: | HPO:0000974 | ||||||||||||
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) Abnormal elasticity of skin(HPO:0010647) Abnormally lax or hyperextensible skin(HPO:0008067) Hyperextensible skin(HPO:0000974) MedDRA: |
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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) |