Disease browser and phenotype portal

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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 ..Child Behavior Disorders (D002653)
Child Nodes:
........Abuse dwarfism syndrome (C535569)
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:	2074
Name:	Child Behavior Disorders
Definition:	Disturbances considered to be pathological based on age and stage appropriateness, e.g., conduct disturbances and anaclitic depression. This concept does not include psychoneuroses, psychoses, or personality disorders with fixed patterns.
Alternative IDs:
ParentIDs:	MESH:D019952
TreeNumbers:	F03.550.300
Synonyms:	Behavior Disorders, Child \|Disorders, Child Behavior
Slim Mappings:	Mental disorder
Reference:	MedGen: D002653 MeSH: D002653 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants