Genopathy
Gene-Disorder Association · Article
Gene
IDH1
Isocitrate Dehydrogenase (NADP(+)) 1
Manually curatedApproved treatment annotated
Association Review

In brief

The association between IDH1 (Isocitrate Dehydrogenase (NADP(+)) 1) and Leukemia, Acute Myeloid is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and causative variation.

Sources 3
Clinical variants 2
Symptoms 5
Compounds 13
Trials 1,028of 4,484 via IDH1 compounds
Publications 2
01
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
02
Provenance

Evidence and sources

3 sources

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

Request access
03
IDH1

The gene

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

Request access
04
Leukemia, Acute Myeloid

The disorder

27 database identifiers

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

Request access
05
Phenotype

Clinical features

1 clinical feature

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
06
ClinVar and variant evidence

Genetic basis

2 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Request access
07
Interventions

Therapeutics

13 compounds & drugs

Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.

Request access
08
Human studies

Clinical trials

4,484 clinical trials

Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.

Request access
09
Literature

Reading

2 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Request access
10
Provenance

References & sources

13 references

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

Request access