Freckling

Symptom Information:

Symptom ID: HPO:0001480
Synonyms:
Freckles [HPO:0001480]
Freckling [OMIM:Freckling]
Freckles [OMIM:Freckles]
Quality:
Cross references:
OMIM: "Freckling" [OMIM:Freckling]
OMIM: "Freckles" [OMIM:Freckles]
UMLS:C0016689 "Freckles" [HPO:0001480]
Is a (Direct Parents):
HPO         Abnormality of skin pigmentation
HPO         Inguinal freckling
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)
                      Freckling(HPO:0001480)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

ADULT syndrome (Orphanet:978)
Cardiospondylocarpofacial syndrome (Orphanet:3238)
Carney complex-trismus-pseudocamptodactyly syndrome (Orphanet:319340)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
NEUROFIBROMATOSIS, FAMILIAL SPINAL (OMIM:162210)
UV-SENSITIVE SYNDROME 1 (OMIM:600630)
UV-SENSITIVE SYNDROME 2 (OMIM:614621)
UV-SENSITIVE SYNDROME 3 (OMIM:614640)
UV-sensitive syndrome (Orphanet:178338)
WAARDENBURG SYNDROME, TYPE 2E (OMIM:611584)
XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD (OMIM:194400)
Xeroderma pigmentosum (Orphanet:910)
Xeroderma pigmentosum complementation group B (Orphanet:276252)