NLGN3, neuroligin 3, 54413

N. diseases: 63; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		0.600 Biomarker disease MGD
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C1845341
Disease: ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder) 		0.600 Biomarker disease CTD_human
CUI: C1845341
Disease: ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder) 		0.600 SusceptibilityMutation disease CLINVAR
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.500 Biomarker disease HPO
CUI: C1845540
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding) 		0.400 SusceptibilityMutation disease CLINVAR
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.130 Biomarker group HPO
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		0.120 GeneticVariation disease CLINVAR
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker phenotype HPO
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		0.100 Biomarker disease HPO
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		0.100 Biomarker phenotype HPO
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		0.100 Biomarker phenotype HPO
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		0.100 CausalMutation disease CLINVAR
CUI: C0877243
Disease: Increased serum serotonin
Increased serum serotonin 		0.100 Biomarker phenotype HPO
CUI: C1837352
Disease: Childhood onset
Childhood onset 		0.100 Biomarker phenotype HPO
CUI: C1837649
Disease: Impaired ability to form peer relationships
Impaired ability to form peer relationships 		0.100 Biomarker phenotype HPO
CUI: C1837650
Disease: Lack of spontaneous play
Lack of spontaneous play 		0.100 Biomarker phenotype HPO
CUI: C1837653
Disease: Inflexible adherence to routines or rituals
Inflexible adherence to routines or rituals 		0.100 Biomarker phenotype HPO
CUI: C1843367
Disease: Poor school performance
Poor school performance 		0.100 CausalMutation phenotype CLINVAR
CUI: C1845337
Disease: Lack of peer relationships
Lack of peer relationships 		0.100 Biomarker phenotype HPO
CUI: C1853237
Disease: Isolated cases
Isolated cases 		0.100 Biomarker phenotype HPO
CUI: C4021798
Disease: Impaired use of nonverbal behaviors
Impaired use of nonverbal behaviors 		0.100 Biomarker phenotype HPO
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior 		0.100 Biomarker phenotype HPO
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma 		0.010 AlteredExpression disease BEFREE Glioblastoma recurrence correlates with NLGN3 levels. 29777576 2018
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma 		0.010 AlteredExpression disease BEFREE Glioblastoma recurrence correlates with NLGN3 levels. 29777576 2018