LAMA1, laminin subunit alpha 1, 284217

N. diseases: 107; N. variants: 21
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4014821
Disease: Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome 		0.610 GeneticVariation disease CLINVAR
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		0.120 Biomarker group HPO
CUI: C0003467
Disease: Anxiety
Anxiety 		0.110 GeneticVariation disease CLINVAR
CUI: C0027092
Disease: Myopia
Myopia 		0.110 Biomarker disease HPO
CUI: C0027092
Disease: Myopia
Myopia 		0.110 CausalMutation disease CLINVAR
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		0.100 CausalMutation phenotype CLINVAR
CUI: C0002418
Disease: Amblyopia
Amblyopia 		0.100 Biomarker phenotype HPO
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 CausalMutation disease CLINVAR
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation disease CLINVAR
CUI: C0017152
Disease: Gastritis
Gastritis 		0.100 GeneticVariation disease CLINVAR
CUI: C0018681
Disease: Headache
Headache 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0027497
Disease: Nausea
Nausea 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0028738
Disease: Nystagmus
Nystagmus 		0.100 Biomarker disease HPO
CUI: C0036572
Disease: Seizures
Seizures 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0038379
Disease: Strabismus
Strabismus 		0.100 Biomarker disease HPO
CUI: C0042454
Disease: Velopharyngeal Insufficiency
Velopharyngeal Insufficiency 		0.100 CausalMutation disease CLINVAR
CUI: C0266491
Disease: Neuronal heterotopia
Neuronal heterotopia 		0.100 Biomarker disease HPO
CUI: C0271270
Disease: Oculovestibuloauditory syndrome
Oculovestibuloauditory syndrome 		0.100 Biomarker disease HPO
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		0.100 CausalMutation phenotype CLINVAR
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		0.100 Biomarker phenotype HPO
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay 		0.100 Biomarker disease HPO
CUI: C0521694
Disease: Atrophic retina
Atrophic retina 		0.100 Biomarker disease HPO
CUI: C0563243
Disease: Poor coordination
Poor coordination 		0.100 CausalMutation phenotype CLINVAR
CUI: C0600104
Disease: Obsessive compulsive behavior
Obsessive compulsive behavior 		0.100 GeneticVariation disease CLINVAR
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.100 GeneticVariation disease CLINVAR