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: digestive system neoplasm (MONDO:0021223)
Parent Node: disease of facial skeleton (MONDO:0023369)
Parent Node: mouth disease (MONDO:0006858)
Parent Node: skull neoplasm (MONDO:0024653)
..Starting node ..neoplasm of jaw ()
Child Nodes:
........benign neoplasm of lower jaw bone ()
........congenital epulis ()
........jaw cancer ()
........maxillary neoplasm ()
........neoplasm of retromolar area ()
Sister Nodes:
..anterior cranial fossa meningioma ()
..cranial nodular fasciitis ()
..jugular foramen meningioma ()
..middle cranial fossa meningioma ()
..neoplasm of jaw ()
..orbit neoplasm ()
..paranasal sinus neoplasm (disease) ()
..posterior cranial fossa meningioma ()
..schwannoma of jugular foramen ()
..skull base neoplasm ()
..skull cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21580
Name:	neoplasm of jaw
Definition:	A neoplasm (disease) that involves the jaw skeleton.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	jaw skeleton neoplasm; jaw skeleton neoplasm (disease); jaw skeleton tumor; neoplasm of jaw skeleton; tumor of jaw skeleton
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal