Periorbital hyperpigmentation

Symptom Information:

Symptom ID: HPO:0001106
Synonyms:
Periorbital hyperpigmentation [OMIM:Periorbital hyperpigmentation]
Quality:
Cross references:
OMIM: "Periorbital hyperpigmentation" [OMIM:Periorbital hyperpigmentation]
Is a (Direct Parents):
HPO         Abnormality of skin pigmentation
HPO         Abnormality of the periorbital region
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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 hyperpigmentation(HPO:0001106)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Abnormality of skin pigmentation(HPO:0001000)
                      Periorbital hyperpigmentation(HPO:0001106)
MedDRA:
Database Frequency: 3 / 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)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)