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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 ..Elimination Disorders (D019960)
Child Nodes:
........Encopresis (D004688) 1
........Enuresis (D004775) 3
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:	3683
Name:	Elimination Disorders
Definition:	Excretory-related psychiatric disorders usually diagnosed in infancy or childhood.
Alternative IDs:
ParentIDs:	MESH:D019952
TreeNumbers:	F03.550.375
Synonyms:	Disorder, Elimination \|Disorders, Elimination \|Elimination Disorder
Slim Mappings:	Mental disorder
Reference:	MedGen: D019960 MeSH: D019960 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants