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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 ..Schizophrenia, Childhood (D012561)
Child Nodes:
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:	10030
Name:	Schizophrenia, Childhood
Definition:	An obsolete concept, historically used for childhood mental disorders thought to be a form of schizophrenia.
Alternative IDs:
ParentIDs:	MESH:D019952
TreeNumbers:	F03.550.768
Synonyms:	Childhood Onset Schizophrenia \|Childhood-Onset Schizophrenia \|Childhood Schizophrenia \|Schizophrenia, Childhood-Onset
Slim Mappings:	Mental disorder
Reference:	MedGen: D012561 MeSH: D012561 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants