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: head and neck cancer (MONDO:0005627)
Parent Node: nasal cavity neoplasm (MONDO:0004756)
Parent Node: respiratory system cancer (MONDO:0000376)
Parent Node: sensory system cancer (MONDO:0000649)
..Starting node ..nasal cavity cancer ()
Child Nodes:
........nasal cavity carcinoma ()
........nasal cavity lymphoma ()
........nasal cavity olfactory neuroblastoma ()
Sister Nodes:
..auditory system cancer ()
..malignant ear neoplasm ()
..nasal cavity cancer ()
..ocular cancer ()
..optic tract astrocytoma ()
..paranasal sinus cancer ()
..tongue cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1128
Name:	nasal cavity cancer
Definition:	A malignant neoplasm involving the nasal cavity
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	cancer of nasal cavity; malignant nasal cavity neoplasm; malignant nasal cavity tumor; malignant neoplasm of nasal cavities; malignant neoplasm of nasal cavity; malignant neoplasm of the nasal cavity; malignant tumor of nasal cavity; malignant tumor of the nasal cavity; nasal cavity cancer
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal