MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation 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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: paranasal sinus neoplasm (disease) (MONDO:0005289)
Parent Node: respiratory system cancer (MONDO:0000376)
Parent Node: sensory system cancer (MONDO:0000649)
Parent Node: skull cancer (MONDO:0002132)
..Starting node ..paranasal sinus cancer ()
Child Nodes:
........paranasal sinus carcinoma ()
........paranasal sinus lymphoma ()
Sister Nodes:
..jaw cancer ()
..malignant jugulotympanic paraganglioma ()
..orbital cancer ()
..paranasal sinus cancer ()
..pituitary cancer ()
..skull base chordoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	20669
Name:	paranasal sinus cancer
Definition:	A primary or metastatic malignant neoplasm involving the paranasal sinuses.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	malignant accessory sinus neoplasm; malignant accessory sinus tumor; malignant neoplasm of accessory sinus; malignant neoplasm of paranasal sinus; malignant neoplasm of the accessory sinus; malignant neoplasm of the paranasal sinus; malignant paranasal sinus neoplasm; malignant paranasal sinus tumor
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal