Genopathy
Gene-Disorder Association · Article
Gene
SAMHD1
SAM And HD Domain Containing Deoxynucleoside Triphosphate Triphosphohydrolase 1
Disorder
Aicardi Syndrome
First reported 1969
Key publication · disorder [Spasma-in-flexion syndrome, callosal agenesis, chorioretinal abnormalities].Archives francaises de pediatrie · 1969
Manually curated
Association Review

In brief

The association between SAMHD1 (SAM And HD Domain Containing Deoxynucleoside Triphosphate Triphosphohydrolase 1) and Aicardi Syndrome is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 116
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

1 source

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

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03
SAMHD1

The gene

1 source summary

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

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04
Aicardi Syndrome

The disorder

11 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

79 clinical features

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

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06
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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07
Provenance

References & sources

7 references

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

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