Genopathy
Gene-Disorder Association · Article
Gene
YWHAZ
Tyrosine 3-Monooxygenase/Tryptophan 5-Monooxygenase Activation Protein Zeta
Disorder
Popov-Chang Syndrome
First reported 2019
Key publication · disorder A YWHAZ Variant Associated With Cardiofaciocutaneous Syndrome Activates the RAF-ERK Pathway.Frontiers in physiology · 2019
Manually curated
Association Review

In brief

The association between YWHAZ (Tyrosine 3-Monooxygenase/Tryptophan 5-Monooxygenase Activation Protein Zeta) and Popov-Chang Syndrome is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and causative variation.

Sources 2
Clinical variants 0
Symptoms 47
Compounds 0
Trials 0
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

2 sources

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

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03
YWHAZ

The gene

2 source summaries

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

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04
Popov-Chang Syndrome

The disorder

3 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

1 clinical feature

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

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06
Provenance

References & sources

4 references

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

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