Soft skin
Symptom Information:
Symptom ID: | HPO:0000977 | ||||||
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) Soft skin(HPO:0000977) MedDRA: |
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Database Frequency: | 23 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA | (OMIM:102100) |
Acromelanosis | (Orphanet:39) |
Aneurysm - osteoarthritis syndrome | (Orphanet:284984) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB | (OMIM:614437) |
Diaphyseal medullary stenosis - bone malignancy | (Orphanet:85182) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
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, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type | (Orphanet:300179) |
Ehlers-Danlos syndrome, kyphoscoliotic type | (Orphanet:1900) |
LOEYS-DIETZ SYNDROME, TYPE 2A | (OMIM:608967) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
Marfan syndrome type 2 | (Orphanet:284973) |
Occipital horn syndrome | (Orphanet:198) |
Renal coloboma syndrome | (Orphanet:1475) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Williams syndrome | (Orphanet:904) |
X-linked Ehlers-Danlos syndrome | (Orphanet:75497) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |