Peripheral artery occlusive disease

Symptom Information:

Symptom ID: HPO:0005315
Synonyms:
Occlusive arterial disease [OMIM:Occlusive arterial disease]
Arterial occlusive disease [MedDRA:10062599]
Quality:
Cross references:
OMIM: "Occlusive arterial disease" [OMIM:Occlusive arterial disease]
Is a (Direct Parents):
HPO         Peripheral arterial disease
MedDRA Non-site specific necrosis and vascular insufficiency NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Abnormality of the systemic arterial tree(HPO:0011004)
                Abnormalities of the peripheral arteries(HPO:0005114)
                   Arterial stenosis(HPO:0100545)
                      Peripheral arterial disease(HPO:0004950)
                         Peripheral artery occlusive disease(HPO:0005315)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216)
       Non-site specific necrosis and vascular insufficiency NEC(MedDRA:10029558)
          Peripheral artery occlusive disease(HPO:0005315)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS (OMIM:134400)
Fabry disease (Orphanet:324)
Hereditary arterial and articular multiple calcification syndrome (Orphanet:289601)
PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE (OMIM:167850)
PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE (OMIM:167850)
Primary hyperoxaluria (Orphanet:416)
Primary hyperoxaluria type 1 (Orphanet:93598)