Premature skin wrinkling

Symptom Information:

Symptom ID: HPO:0100678
Synonyms:
Wrinkled skin [HPO:0100678]
Wrinkled skin [Orphanet:23150]
Wrinkled skin (finding) [Orphanet:23150]
Skin Wrinkling [Orphanet:23150]
Rippled skin [Orphanet:23150]
Skin wrinkling [HPO:0100678]
Skin wrinkling [Orphanet:23150]
Skin wrinkling [MedDRA:10040954]
Wrinkles [MedDRA:10040954]
Wrinkling [MedDRA:10040954]
Glabellar frown lines [MedDRA:10040954]
Frown lines [MedDRA:10040954]
Crow's feet [MedDRA:10040954]
Quality:
Cross references:
HPO:0007392 "Excessive wrinkled skin" [Orphanet:23150]
Orphanet:23150 "Rippled skin" [Orphanet:23150]
UMLS:C0037301 "Skin Wrinkling" [Orphanet:23150]
Is a (Direct Parents):
HPO         Prematurely aged appearance
MedDRA Skin dystrophies
Orphanet Abnormality of the skin
HPO         Abnormality of skin morphology
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)
                   Premature skin wrinkling(HPO:0100678)
                Prematurely aged appearance(HPO:0007495)
                   Premature skin wrinkling(HPO:0100678)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cornification and dystrophic skin disorders(MedDRA:10011063)
       Skin dystrophies(MedDRA:10040837)
          Premature skin wrinkling(HPO:0100678)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

Ablepharon macrostomia syndrome (Orphanet:920)
Acrogeria (Orphanet:2500)
CUTIS LAXA, AUTOSOMAL DOMINANT 2 (OMIM:614434)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cutis laxa (Orphanet:209)
DERMATOLEUKODYSTROPHY (OMIM:221790)
Ehlers-Danlos syndrome type 7B (Orphanet:99876)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Focal facial dermal dysplasia (Orphanet:79133)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
LMNA-related cardiocutaneous progeria syndrome (Orphanet:363618)
Leprechaunism (Orphanet:508)
MMEP syndrome (Orphanet:3434)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
Pseudoxanthoma elasticum (Orphanet:758)
Rabson-Mendenhall syndrome (Orphanet:769)
SHORT syndrome (Orphanet:3163)
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus (Orphanet:137608)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)