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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 ..Motor Skills Disorders (D019957)
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:	7398
Name:	Motor Skills Disorders
Definition:	Marked impairments in the development of motor coordination such that the impairment interferes with activities of daily living. (From DSM-IV, 1994)
Alternative IDs:
ParentIDs:	MESH:D019952
TreeNumbers:	F03.550.650
Synonyms:	Coordination Disorder, Developmental \|Developmental Coordination Disorder \|Developmental Coordination Disorders \|Motor Skills Disorder
Slim Mappings:	Mental disorder
Reference:	MedGen: D019957 MeSH: D019957 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants