Hypoalphalipoproteinemia

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 9
OrphanetNr: 31153
OMIM Id:
ICD-10: E78.6
UMLs: C0473527
MeSH: D052456
MedDRA: 10065156
Snomed: 190785000

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Rare hypolipidemia
 -Rare endocrine disease
 -Rare genetic disease

Symptom Information: Sort by abundance 

1
 (HPO:0000481) Abnormality of the cornea Very frequent [Orphanet] 124 / 7739
2
 (HPO:0011675) Arrhythmia Occasional [Orphanet] 226 / 7739
3
 (HPO:0002140) Ischemic stroke Very frequent [Orphanet] 70 / 7739
4
 (HPO:0002621) Atherosclerosis Very frequent [Orphanet] 33 / 7739
5
 (HPO:0001695) Cardiac arrest Occasional [Orphanet] 87 / 7739
6
 (HPO:0001677) Coronary artery disease Very frequent [Orphanet] 58 / 7739
7
 (HPO:0003119) Abnormality of lipid metabolism Very frequent [Orphanet] 60 / 7739
8
 (HPO:0001012) Multiple lipomas Very frequent [Orphanet] 43 / 7739
9
 (HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: