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: ethmoidal sinus neoplasm (MONDO:0001764)
Parent Node: respiratory system benign neoplasm (MONDO:0000382)
Parent Node: sensory organ benign neoplasm (MONDO:0000633)
..Starting node ..benign neoplasm of ethmoidal sinus ()
Child Nodes:
........ethmoid 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:	21515
Name:	benign neoplasm of ethmoidal sinus
Definition:	A benign neoplasm that involves the ethmoid sinus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign ethmoid sinus neoplasm; benign ethmoid sinus tumor; benign ethmoidal sinus neoplasm; benign ethmoidal sinus tumor; benign neoplasm of ethmoid sinus; benign neoplasm of the ethmoid sinus; benign neoplasm of the ethmoidal sinus; benign tumor of ethmoid sinus; benign tumor of ethmoidal sinus; be
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal