MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: nasal cavity neoplasm (MONDO:0004756)
Parent Node: respiratory system benign neoplasm (MONDO:0000382)
Parent Node: sensory organ benign neoplasm (MONDO:0000633)
..Starting node ..benign neoplasm of nasal cavity ()
Child Nodes:
........nasal vestibule squamous 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:	21475
Name:	benign neoplasm of nasal cavity
Definition:	A benign neoplasm that involves the nasal cavity.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign nasal cavity neoplasm; benign nasal cavity tumor; benign neoplasm of the nasal cavity; benign tumor of nasal cavity; benign tumor of the nasal cavity; nasal cavity benign neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal