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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 ..Anxiety, Separation (D001010)
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:	774
Name:	Anxiety, Separation
Definition:	Anxiety experienced by an individual upon separation from a person or object of particular significance to him.
Alternative IDs:
ParentIDs:	MESH:D019952
TreeNumbers:	F03.550.075
Synonyms:	Anxiety Disorder, Separation \|Separation Anxiety \|Separation Anxiety Disorder
Slim Mappings:	Mental disorder
Reference:	MedGen: D001010 MeSH: D001010 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants