Hypermelanotic macule

Symptom Information:

Symptom ID: HPO:0001034
Synonyms:
Hyperpigmented macules [HPO:0001034]
Hyperpigmented skin patches [HPO:0001034]
Hyperpigmented spots [HPO:0001034]
Hyperpigmented macules [OMIM:Hyperpigmented macules]
Hyperpigmented spots [OMIM:Hyperpigmented spots]
Hyperpigmented skin patches (face, neck, trunk, limbs, lip, oral mucosa, palms, and soles) [OMIM:Hyperpigmented skin patches (face, neck, trunk, limbs, lip, oral mucosa, palms, and soles)]
Quality:
Cross references:
OMIM: "Hyperpigmented macules" [OMIM:Hyperpigmented macules]
OMIM: "Hyperpigmented spots" [OMIM:Hyperpigmented spots]
OMIM: "Hyperpigmented skin patches (face, neck, trunk, limbs, lip, oral mucosa, palms, and soles)" [OMIM:Hyperpigmented skin patches (face, neck, trunk, limbs, lip, oral mucosa, palms, and soles)]
Is a (Direct Parents):
HPO         Irregular hyperpigmentation
HPO         Localized skin lesion
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)
                            Hypermelanotic macule(HPO:0001034)
             Localized skin lesion(HPO:0011355)
                Hypermelanotic macule(HPO:0001034)
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Blue rubber bleb nevus (Orphanet:1059)
Constitutional mismatch repair deficiency syndrome (Orphanet:252202)
Darier disease (Orphanet:218)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
Familial progressive hyperpigmentation (Orphanet:79146)
HAIRY PALMS AND SOLES (OMIM:139650)
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE (OMIM:145250)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Hypo- and hypermelanotic cutaneous macules - retarded growth - intellectual deficiency (Orphanet:2435)
Kaposi's sarcoma (Orphanet:33276)
LENTIGINOSIS, INHERITED PATTERNED (OMIM:151001)
Leigh syndrome (Orphanet:506)
Leprechaunism (Orphanet:508)
Lymphangioleiomyomatosis (Orphanet:538)
Maculopapular cutaneous mastocytosis (Orphanet:79457)
Non-polyposis Turcot syndrome (Orphanet:99817)
Peutz-Jeghers syndrome (Orphanet:2869)
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION (OMIM:607944)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Torg-Winchester syndrome (Orphanet:3460)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)