Multiple lentigines
Symptom Information:
Symptom ID: | HPO:0001003 | ||
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) 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: |
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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) |