Disease #00147 (FHBL1 (HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1), OMIM:615558)

Official abbreviation FHBL1
Name HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1
OMIM ID 615558
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene APOB
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-22 10:10:04 +00:00 (UTC)
Date last edited N/A

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