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: frontal sinus neoplasm (MONDO:0001757)
Parent Node: respiratory system benign neoplasm (MONDO:0000382)
Parent Node: sensory organ benign neoplasm (MONDO:0000633)
..Starting node ..benign neoplasm of frontal sinus ()
Child Nodes:
........frontal 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:	21483
Name:	benign neoplasm of frontal sinus
Definition:	A benign neoplasm that involves the frontal sinus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign frontal sinus neoplasm; benign frontal sinus tumor; benign neoplasm of the frontal sinus; benign tumor of frontal sinus; benign tumor of the frontal sinus; frontal sinus benign neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal