Genopathy
Gene-Disorder Association · Article
Gene
CRIPTO
Cripto, EGF-CFC Family Member
Disorder
Absent Septum Pellucidum
First reported 1954
Key publication · disorder An unusual congenital anomaly of the brain: agenesis of the corpus callosum, absence of the septum pellucidum, and fusion of the cerebral hemispheres.Journal of neuropathology and experimental neurology · 1954
Manually curated
Association Review

In brief

The association between CRIPTO (Cripto, EGF-CFC Family Member) and Absent Septum Pellucidum is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
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
CRIPTO

The gene

1 source summary

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

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04
Absent Septum Pellucidum

The disorder

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

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05
Provenance

References & sources

2 references

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

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