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 carcinoma (MONDO:0000380)
Parent Node: sphenoidal sinus neoplasm (MONDO:0004047)
..Starting node ..sphenoidal sinus cancer ()
Child Nodes:
........sphenoid sinus squamous cell carcinoma ()
Sister Nodes:
..benign neoplasm of sphenoidal sinus ()
..polyp of sphenoidal sinus ()
..sphenoidal sinus cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1994
Name:	sphenoidal sinus cancer
Definition:	A malignant neoplasm involving the sphenoidal sinus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	cancer of sphenoidal sinus; malignant neoplasm of sphenoid sinus; malignant neoplasm of sphenoidal sinus; malignant neoplasm of the sphenoid sinus; malignant neoplasm of the sphenoidal sinus; malignant sphenoid sinus neoplasm; malignant sphenoid sinus tumor; malignant sphenoidal sinus neoplasm; mali
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal