Freckling
Symptom Information:
Symptom ID: | HPO:0001480 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |