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Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

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ADAM10 and neurodevelopmental disorder are reported together in 1 article.

Gene

ADAM10

10articles

10mentions

0variants with confirmed gene link

Most co-reported phenotypes (articles)

Phenotype

450articles

450mentions

12co-reported genes shown

Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

1 records shown · first 60

PMID 39588547 | PMCID PMC11586360 | DOI 10.3389/fpsyt.2024.1495017 · Frontiers in psychiatry · 2024 · 5 validated mentions

Evidence preview

Type	Entity	Source evidence	Confidence	Extractor
gene	ADAM10	“It also discusses the possible involvement of the retina and molecular biomarkers, specifically Disintegrin and metalloproteinase domain-containing protein 10 (ADAM10) and ciliary neurotrophic factor (CNTF) in the pathophysiology of SSD and ASD.”	0.98	hgnc_dict_v1
phenotype	neurodevelopmental disorder	“Schizophrenia and Autism spectrum disorders (SSD and ASD) are neurodevelopmental disorders involving cognitive impairment.”	0.93	phenotype_alias_lexicon_v2
gene	CNTF	“It also discusses the possible involvement of the retina and molecular biomarkers, specifically Disintegrin and metalloproteinase domain-containing protein 10 (ADAM10) and ciliary neurotrophic factor (CNTF) in the pathophysiology of SSD and ASD.”	0.98	hgnc_dict_v1
phenotype	intellectual disability	“Molecular physiology unlocks the mystery that relates cognitive impairment with the retina in schizophrenia and autism spectrum disorders: a perspective review.”	0.93	phenotype_alias_lexicon_v2