Lack of skin elasticity
Symptom Information:
Symptom ID: | HPO:0100679 | |||||||
Synonyms: |
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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) 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) |
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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) |