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: Female Urogenital Diseases and Pregnancy Complications (D005261)
..Starting node ..Pregnancy Complications (D011248)
Child Nodes:
........Abortion, Spontaneous (D000022) 9
........Acute fatty liver of pregnancy (C537957)
........Chorea Gravidarum (D020150)
........Diabetes, Gestational (D016640) 5
........Fetal Death (D005313) 4
........Fetal Diseases (D005315) 51
........Hypertension, Pregnancy-Induced (D046110) 7
........Hyperthyroidism, Familial Gestational (C566384)
........Intrahepatic Cholestasis of Pregnancy (C535932)
........Maternal Death (D063130)
........Morning Sickness (D048968) 1
........Nuchal Cord (D053589)
........Obstetric Labor Complications (D007744) 17
........Oligohydramnios (D016104) 1
........Pelvic Floor Disorders (D059952)
........Pemphigoid Gestationis (D006559)
........Perinatal Death (D066087)
........Phenylketonuria, Maternal (D017042)
........Placenta Diseases (D010922) 6
........Polyhydramnios (D006831) 4
........Pregnancy Complications, Cardiovascular (D011249) 1
........Pregnancy Complications, Hematologic (D011250)
........Pregnancy Complications, Infectious (D011251) 4
........Pregnancy Complications, Neoplastic (D011252) 7
........Pregnancy in Diabetics (D011254) 6
........Pregnancy, Ectopic (D011271) 7
........Pregnancy, Prolonged (D011273)
........Prenatal Injuries (D049188) 1
........Pruritic urticarial papules plaques of pregnancy (C535817)
........Puerperal Disorders (D011644) 13
........Twinning due to Superfetation (C566018)
Sister Nodes:
..Female Urogenital Diseases (D052776) 815
..Pregnancy Complications (D011248) 156
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9224
Name:	Pregnancy Complications
Definition:	Conditions or pathological processes associated with pregnancy. They can occur during or after pregnancy, and range from minor discomforts to serious diseases that require medical interventions. They include diseases in pregnant females, and pregnancies in females with diseases.
Alternative IDs:
ParentIDs:	MESH:D005261
TreeNumbers:	C13.703
Synonyms:	Complication, Pregnancy \|Complications, Pregnancy \|Pregnancy Complication
Slim Mappings:	Pregnancy complication
Reference:	MedGen: D011248 MeSH: D011248 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants