NLGN3, neuroligin 3, 54413

N. diseases: 63; N. variants: 7
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1845341
Disease: ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder) 		disease Disease or Syndrome 1 1 0.600 None 1.000 1 1 2003 2003
CUI: C1845540
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding) 		disease Finding 1 1 0.400 None 1.000 1 1 2003 2003
CUI: C0426317
Disease: Genitourinary symptoms
Genitourinary symptoms 		phenotype Sign or Symptom 2 1 0.010 None 1.000 1 1 2019 2019
CUI: C1837649
Disease: Impaired ability to form peer relationships
Impaired ability to form peer relationships 		phenotype Mental Disorders Mental or Behavioral Dysfunction 3 0.100 None 0
CUI: C1845337
Disease: Lack of peer relationships
Lack of peer relationships 		phenotype Mental Disorders Finding 3 0.100 None 0
CUI: C1837650
Disease: Lack of spontaneous play
Lack of spontaneous play 		phenotype Behavior and Behavior Mechanisms Finding 5 1 0.100 None 0
CUI: C1837653
Disease: Inflexible adherence to routines or rituals
Inflexible adherence to routines or rituals 		phenotype Behavior and Behavior Mechanisms Finding 5 1 0.100 None 0
CUI: C4726566
Disease: Extracranial Solid Neoplasm
Extracranial Solid Neoplasm 		disease Neoplastic Process 8 0.010 None < 0.001 1 2019 2019
CUI: C0877243
Disease: Increased serum serotonin
Increased serum serotonin 		phenotype Finding 8 0.100 None 0
CUI: C4021798
Disease: Impaired use of nonverbal behaviors
Impaired use of nonverbal behaviors 		phenotype Mental Disorders Mental or Behavioral Dysfunction 8 5 0.100 None 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior 		phenotype Mental or Behavioral Dysfunction 13 0.100 None 0
CUI: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction 		phenotype Digestive System Diseases Disease or Syndrome 16 6 0.010 None 1.000 1 1 2019 2019
CUI: C0150080
Disease: Social Communication Disorder
Social Communication Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 40 4 0.010 None 1.000 1 1 2017 2017
CUI: C1837352
Disease: Childhood onset
Childhood onset 		phenotype Finding 56 0.100 None 0
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		phenotype Sign or Symptom 69 23 0.010 None 1.000 1 2017 2017
CUI: C2986658
Disease: Diffuse Intrinsic Pontine Glioma
Diffuse Intrinsic Pontine Glioma 		disease Neoplastic Process 87 9 0.010 None 1.000 1 2017 2017
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 94 48 0.010 None 1.000 1 1 2010 2010
CUI: C1849265
Disease: Overgrowth
Overgrowth 		phenotype Finding 103 93 0.100 None 1.000 4 1 2003 2014
CUI: C1853237
Disease: Isolated cases
Isolated cases 		phenotype Finding 111 0.100 None 0
CUI: C0149940
Disease: Sciatic Neuropathy
Sciatic Neuropathy 		disease Nervous System Diseases Disease or Syndrome 115 0.200 None 1.000 1 2007 2007
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		disease Behavior and Behavior Mechanisms Individual Behavior 135 0.100 None 0
CUI: C4722099
Disease: High grade glioma
High grade glioma 		disease Neoplasms Neoplastic Process 190 15 0.010 None 1.000 1 2017 2017
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		phenotype Mental Disorders Mental or Behavioral Dysfunction 192 26 0.100 None 0
CUI: C0013170
Disease: Drug habituation
Drug habituation 		phenotype Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 196 19 0.010 None 1.000 1 2020 2020
CUI: C1843367
Disease: Poor school performance
Poor school performance 		phenotype Finding 211 411 0.100 None 0 1