Soft skin

Symptom Information:

Symptom ID: HPO:0000977
Synonyms:
Velvety skin [HPO:0000977]
VELVETY SKIN TEXTURE [HPO:0000977]
Soft skin [OMIM:Soft skin]
Velvety skin [OMIM:Velvety skin]
Velvety skin texture [OMIM:Velvety skin texture]
Skin velvety [OMIM:Skin velvety]
Quality:
Cross references:
OMIM: "Soft skin" [OMIM:Soft skin]
OMIM: "Velvety skin" [OMIM:Velvety skin]
OMIM: "Velvety skin texture" [OMIM:Velvety skin texture]
OMIM: "Skin velvety" [OMIM:Skin velvety]
Is a (Direct Parents):
HPO         Abnormal elasticity of 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)
                      Soft skin(HPO:0000977)
MedDRA:
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)