Multiple lentigines

Symptom Information:

Symptom ID: HPO:0001003
Synonyms:
Multiple lentigines [OMIM:Multiple lentigines]
Quality:
Cross references:
OMIM: "Multiple lentigines" [OMIM:Multiple lentigines]
Is a (Direct Parents):
HPO         Hypermelanotic macule
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Localized skin lesion(HPO:0011355)
                Hypermelanotic macule(HPO:0001034)
                   Multiple lentigines(HPO:0001003)
             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)
                               Multiple lentigines(HPO:0001003)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Arterial dissection - lentiginosis (Orphanet:1682)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carney complex (Orphanet:1359)
Gastrocutaneous syndrome (Orphanet:2069)
LEOPARD SYNDROME 2 (OMIM:611554)
LEOPARD SYNDROME 3 (OMIM:613707)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
Ocular albinism with congenital sensorineural deafness (Orphanet:352740)