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: bone benign neoplasm (MONDO:0000631)
Parent Node: glandular papilloma (MONDO:0021078)
Parent Node: paranasal sinus neoplasm (disease) (MONDO:0005289)
Parent Node: respiratory system benign neoplasm (MONDO:0000382)
Parent Node: sensory organ benign neoplasm (MONDO:0000633)
..Starting node ..paranasal sinus Schneiderian papilloma ()
Child Nodes:
........ethmoid sinus Schneiderian papilloma ()
........frontal sinus Schneiderian papilloma ()
........maxillary sinus Schneiderian papilloma ()
........sphenoid 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:	6353
Name:	paranasal sinus Schneiderian papilloma
Definition:	A papilloma that arises from the ciliated respiratory mucosa that lines the paranasal sinuses. It is classified as inverted papilloma and oncocytic papilloma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	accessory sinus Schneiderian papilloma; paranasal sinus Schneiderian papilloma; Schneiderian papilloma of accessory sinus; Schneiderian papilloma of paranasal sinus; Schneiderian papilloma of the accessory sinus; Schneiderian papilloma of the paranasal sinus
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal