Atheroeruptive xanthoma
Symptom Information:
Symptom ID: | HPO:0001039 | |||||
Synonyms: |
|
|||||
Quality: | ||||||
Cross references: |
|
|||||
Is a (Direct Parents): |
|
|||||
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) Xanthomatosis(HPO:0000991) Atheroeruptive xanthoma(HPO:0001039) MedDRA: |
|||||
Database Frequency: | 9 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
GLYCOGEN STORAGE DISEASE Ic | (OMIM:232240) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
HYPERLIPOPROTEINEMIA, TYPE IV | (OMIM:144600) |
HYPERTRIGLYCERIDEMIA, FAMILIAL | (OMIM:145750) |
Hyperlipoproteinemia type 4 | (Orphanet:413) |
Niemann-Pick disease type A | (Orphanet:77292) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |