Atheroeruptive xanthoma

Symptom Information:

Symptom ID: HPO:0001039
Synonyms:
Xanthoma [HPO:0001039]
Atheroeruptive xanthoma [OMIM:Atheroeruptive xanthoma]
Xanthoma [OMIM:Xanthoma]
Xanthomas [OMIM:Xanthomas]
Xanthomas (in some patients) [OMIM:Xanthomas (in some patients)]
Quality:
Cross references:
OMIM: "Atheroeruptive xanthoma" [OMIM:Atheroeruptive xanthoma]
OMIM: "Xanthoma" [OMIM:Xanthoma]
OMIM: "Xanthomas" [OMIM:Xanthomas]
OMIM: "Xanthomas (in some patients)" [OMIM:Xanthomas (in some patients)]
UMLS:C0302314 "Xanthoma" [HPO:0001039]
Is a (Direct Parents):
HPO         Xanthomatosis
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)