Reticular hyperpigmentation

Symptom Information:

Symptom ID: HPO:0007588
Synonyms:
Reticulate hyperpigmentation [HPO:0007588]
Reticular skin hyperpigmentation [Orphanet:23540]
Reticulate hyperpigmentation [OMIM:Reticulate hyperpigmentation]
Irregular/in bands/reticular skin hyperpigmentation [Orphanet:23540]
Reticular hyperpigmentation (neck) [OMIM:Reticular hyperpigmentation (neck)]
Reticulate hyperpigmentation (periocular, perioral, chest, neck, abdomen) [OMIM:Reticulate hyperpigmentation (periocular, perioral, chest, neck, abdomen)]
Reticulate hyperpigmentation (primarily trunk) [OMIM:Reticulate hyperpigmentation (primarily trunk)]
Band skin hyperpigmentation [Orphanet:23540]
Quality:
Cross references:
HPO:0007427 "Reticulated skin pigmentation" [Orphanet:23540]
Orphanet:23540 "Irregular/in bands/reticular skin hyperpigmentation" [Orphanet:23540]
OMIM: "Reticulate hyperpigmentation" [OMIM:Reticulate hyperpigmentation]
OMIM: "Reticular hyperpigmentation (neck)" [OMIM:Reticular hyperpigmentation (neck)]
OMIM: "Reticulate hyperpigmentation (periocular, perioral, chest, neck, abdomen)" [OMIM:Reticulate hyperpigmentation (periocular, perioral, chest, neck, abdomen)]
OMIM: "Reticulate hyperpigmentation (primarily trunk)" [OMIM:Reticulate hyperpigmentation (primarily trunk)]
Is a (Direct Parents):
Orphanet Abnormality of skin pigmentation
HPO         Irregular hyperpigmentation
Orphanet Irregular hyperpigmentation
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)
                   Abnormality of skin pigmentation(HPO:0001000)
                      Hyperpigmentation of the skin(HPO:0000953)
                         Irregular hyperpigmentation(HPO:0007400)
                            Reticular hyperpigmentation(HPO:0007588)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Bloom syndrome (Orphanet:125)
DOWLING-DEGOS DISEASE 2 (OMIM:615327)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
Dermatopathia pigmentosa reticularis (Orphanet:86920)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
Dyskeratosis congenita (Orphanet:1775)
Focal dermal hypoplasia (Orphanet:2092)
Naegeli-Franceschetti-Jadassohn syndrome (Orphanet:69087)
Pilodental dysplasia - refractive errors (Orphanet:2892)