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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Mental Disorders Diagnosed in Childhood (D019952)
..Starting node ..Attention Deficit and Disruptive Behavior Disorders (D019958)
Child Nodes:
........Attention Deficit Disorder with Hyperactivity (D001289) 1
........Conduct Disorder (D019955)
Sister Nodes:
..Anxiety, Separation (D001010)
..Attention Deficit and Disruptive Behavior Disorders (D019958) 3
..Child Behavior Disorders (D002653) 1
..Child Development Disorders, Pervasive (D002659) 12
..Communication Disorders (D003147) 57
..Developmental Disabilities (D002658) 39
..Elimination Disorders (D019960) 6
..Feeding and Eating Disorders of Childhood (D019959)
..Intellectual Disability (D008607) 579
..Learning Disorders (D007859) 12
..Motor Skills Disorders (D019957)
..Mutism (D009155)
..Reactive Attachment Disorder (D019962)
..Schizophrenia, Childhood (D012561)
..Stereotypic Movement Disorder (D019956) 1
..Tic Disorders (D013981) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1051
Name:	Attention Deficit and Disruptive Behavior Disorders
Definition:
Alternative IDs:
ParentIDs:	MESH:D019952
TreeNumbers:	F03.550.150
Synonyms:	Behavior Disorder, Disruptive \|Defiant Disorder, Oppositional \|Disruptive Behavior Disorder \|Oppositional Defiant Disorder
Slim Mappings:	Mental disorder
Reference:	MedGen: D019958 MeSH: D019958 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants