Disease browser and phenotype portal

About
MSeqDR-LSDB
Tools
- Quick-Mitome for WES
- Quick-Mitome
- Quick-Mitome Report
- mtDNA Tool:
- mvTool
- Phy-Mer
- MToolBox
- mvTool for Haplogroup
- mvTool with HmtDB
- MitoMaster
- MitoTIP tRNA Scoring
- MSeq-OpenCGA
- Variant Tool:
- VariantOneStop
- HBCR Exome (Retired)
- POLG Patho. Server
- Data - Awsomics GeEx
- Expert Panel
- Panel Tool:
- Gene Panel Examiner
- Transgenomic_NuclearMitome
- Pedigree Maker
- json2table
Phenome-Disease
Collaboration
- Genesis (GEM.App)
- LeighMap
- Expert Panel
- Collaboration Zone
Submission
- Submit_Interpret_Variant
- Instructions

Hello! Guest! Please Login or Register! Clinician Mode

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

Hearing Loss Disease Portal

Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes

Disease Browser
Parent Node: Mental Disorders (D001523)
..Starting node ..Mental Disorders Diagnosed in Childhood (D019952)
Child 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
Sister Nodes:
..Adjustment Disorders (D000275)
..Anxiety Disorders (D001008) 15
..Chromosome 18 Pericentric Inversion (C563734)
..Delirium, Dementia, Amnestic, Cognitive Disorders (D019965) 100
..Dissociative Disorders (D004213) 1
..Eating Disorders (D001068) 6
..Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders (C564505)
..Factitious Disorders (D005162) 3
..Fragile Site 16p12 (C565001)
..Hydrocephalus, Skeletal Anomalies, and Mental Disturbance (C563413)
..Impulse Control Disorders (D007174) 4
..Mental Disorders Diagnosed in Childhood (D019952) 693
..Mood Disorders (D019964) 23
..Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders (C565786)
..Neurotic Disorders (D009497)
..Personality Disorders (D010554) 12
..Renal Tubular Acidosis, Distal, With Nephrocalcinosis, Short Stature, Mental Retardation, And Distinctive Facies (C566918)
..Schizophrenia and Disorders with Psychotic Features (D019967) 15
..Sexual and Gender Disorders (D019968) 123
..Sleep Disorders (D012893) 41
..Somatoform Disorders (D013001) 4
..Spongiform Encephalopathy with Neuropsychiatric Features (C564678)
..Substance-Related Disorders (D019966) 38
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6966
Name:	Mental Disorders Diagnosed in Childhood
Definition:	Those psychiatric disorders usually first diagnosed in infancy, childhood, or adolescence. These disorders can also be first diagnosed during other life stages.
Alternative IDs:
ParentIDs:	MESH:D001523
TreeNumbers:	F03.550
Synonyms:	Child Mental Disorder \|Child Mental Disorders \|Disorder, Child Mental \|Disorders, Child Mental \|Disorders Usually Diagnosed in Infancy, Childhood or Adolescence \|Mental Disorder, Child \|Mental Disorders, Child
Slim Mappings:	Mental disorder
Reference:	MedGen: D019952 MeSH: D019952 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants