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: bone benign neoplasm (MONDO:0000631)
Parent Node: maxillary sinus neoplasm (MONDO:0006850)
Parent Node: respiratory system benign neoplasm (MONDO:0000382)
Parent Node: sensory organ benign neoplasm (MONDO:0000633)
..Starting node ..benign neoplasm of maxillary sinus ()
Child Nodes:
........maxillary sinus Schneiderian papilloma ()
Sister Nodes:
..benign neoplasm of ear ()
..benign neoplasm of ethmoidal sinus ()
..benign neoplasm of eye ()
..benign neoplasm of frontal sinus ()
..benign neoplasm of maxillary sinus ()
..benign neoplasm of nasal cavity ()
..benign neoplasm of sphenoidal sinus ()
..benign neoplasm of tongue ()
..paranasal sinus Schneiderian papilloma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21484
Name:	benign neoplasm of maxillary sinus
Definition:	A benign neoplasm that involves the maxillary sinus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign maxillary antrum neoplasm; benign maxillary antrum tumor; benign maxillary sinus neoplasm; benign maxillary sinus tumor; benign maxillofacial sinus neoplasm; benign maxillofacial sinus tumor; benign neoplasm of maxillary antrum; benign neoplasm of maxillofacial sinus; benign neoplasm of the m
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal