- 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
- Submission
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
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Human Disease and Phenotype Search
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| 1 | Input Term | OMIM ID | OMIM Disorder | Gene | MESH | Top Match |
| Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release. | ||||||
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