Genopathy
Gene-Disorder Association · Article
Gene
PKM
Pyruvate Kinase M1/2
Manually curatedApproved treatment annotated
Association Review

In brief

The association between PKM (Pyruvate Kinase M1/2) and Anemia, Congenital, Nonspherocytic Hemolytic, 2 is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 38
Compounds 1
Trials 7of 28 via PKM compounds
Publications 0
01
At a glance

Association overview

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

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02
Provenance

Evidence and sources

1 source

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

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03
PKM

The gene

1 source summary

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

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04
Anemia, Congenital, Nonspherocytic Hemolytic, 2

The disorder

14 database identifiers

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

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05
Phenotype

Clinical features

26 clinical features

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

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06
Interventions

Therapeutics

1 compound or drug

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

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07
Human studies

Clinical trials

28 clinical trials

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

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08
Provenance

References & sources

8 references

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

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