Lack of skin elasticity

Symptom Information:

Symptom ID: HPO:0100679
Synonyms:
Tight skin [HPO:0100679]
Stretched skin (finding) [Orphanet:23450]
Stretched skin [Orphanet:23450]
Skin tightness [Orphanet:23450]
Tight skin [OMIM:Tight skin]
Tight skin/lack of elasticity [Orphanet:23450]
Skin tightness [MedDRA:10050637]
Quality:
Cross references:
Orphanet:23450 "Tight skin/lack of elasticity" [Orphanet:23450]
OMIM: "Tight skin" [OMIM:Tight skin]
UMLS:C0558242 "Stretched skin" [Orphanet:23450]
UMLS:C0241166 "Skin tightness" [Orphanet:23450]
Is a (Direct Parents):
Orphanet Abnormality of the skin
MedDRA Dermal and epidermal conditions NEC
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)
                      Lack of skin elasticity(HPO:0100679)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Epidermal and dermal conditions(MedDRA:10014982)
       Dermal and epidermal conditions NEC(MedDRA:10012424)
          Lack of skin elasticity(HPO:0100679)
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

8q22.1 microdeletion syndrome (Orphanet:178303)
Antisynthetase syndrome (Orphanet:81)
Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
CREST syndrome (Orphanet:90290)
Classical phenylketonuria (Orphanet:79254)
Costello syndrome (Orphanet:3071)
Cutis laxa (Orphanet:209)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
Geleophysic dysplasia (Orphanet:2623)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Lamellar ichthyosis (Orphanet:313)
Ledderhose disease (Orphanet:199251)
Leri pleonosteosis (Orphanet:2900)
Lethal restrictive dermopathy (Orphanet:1662)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Mandibular hypoplasia-deafness-progeroid syndrome (Orphanet:363649)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 2 (Orphanet:580)
Neu-Laxova syndrome (Orphanet:2671)
Palmoplantar keratoderma-sclerodactyly syndrome (Orphanet:384)
Pseudoxanthoma elasticum (Orphanet:758)
Reynolds syndrome (Orphanet:779)
Scleroderma (Orphanet:801)
Stiff skin syndrome (Orphanet:2833)
Werner syndrome (Orphanet:902)
Wrinkly skin syndrome (Orphanet:2834)