Periorbital wrinkles

Symptom Information:

Symptom ID: HPO:0000607
Synonyms:
Excess periorbital skin wrinkling [HPO:0000607]
Periorbital wrinkling [HPO:0000607]
Excess periorbital skin wrinkling [OMIM:Excess periorbital skin wrinkling]
Periorbital wrinkles [OMIM:Periorbital wrinkles]
Periorbital wrinkling [OMIM:Periorbital wrinkling]
Quality:
Cross references:
OMIM: "Excess periorbital skin wrinkling" [OMIM:Excess periorbital skin wrinkling]
OMIM: "Periorbital wrinkles" [OMIM:Periorbital wrinkles]
OMIM: "Periorbital wrinkling" [OMIM:Periorbital wrinkling]
Is a (Direct Parents):
HPO         Abnormality of the periorbital region
HPO         Premature skin wrinkling
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)
                      Periorbital wrinkles(HPO:0000607)
                Prematurely aged appearance(HPO:0007495)
                   Premature skin wrinkling(HPO:0100678)
                      Periorbital wrinkles(HPO:0000607)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the periorbital region(HPO:0000606)
                   Periorbital wrinkles(HPO:0000607)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:224900)
Eyebrow duplication - syndactyly (Orphanet:3172)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)