HYPLIP2 and Hyperlipidemia, Familial Combined, 2: Association Evidence

Gene-Disorder Association · Article

Gene

HYPLIP2

Hyperlipidemia, Combined, 2

Disorder

First reported 1974

Key publication · disorder Familial hypercholesterolemia (one form of familial type II hyperlipoproteinemia). A study of its biochemical, genetic and clinical presentation in childhood.The Journal of clinical investigation · 1974

Manually curated

Association Review

In brief

The association between HYPLIP2 (Hyperlipidemia, Combined, 2) and Hyperlipidemia, Familial Combined, 2 is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1

Clinical variants 0

Symptoms 0

Compounds 0

Trials 0

Publications 0

At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access

Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

Request access

Hyperlipidemia, Familial Combined, 2

The disorder

4 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access

Provenance

References & sources

1 reference

Every source and publication cited across this dossier, as one numbered reference list.

Request access