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: dermatophytosis (MONDO:0004678)
Parent Node: face disease (MONDO:0044987)
..Starting node ..tinea barbae ()
Child Nodes:
Sister Nodes:
..adenoid hypertrophy ()
..buccal mucosa neoplasm ()
..cavernous hemangioma of face ()
..disease of facial skeleton ()
..disease of orbital region ()
..facial dermoid cyst ()
..facial paralysis ()
..lipoma of face ()
..nose disease ()
..orofacial cleft ()
..palatal neoplasm ()
..parotid disease ()
..tinea barbae ()
..upper gum cancer ()
..upper lip cancer ()
..uvulitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	242
Name:	tinea barbae
Definition:	A dermatophytosis that involves the beard.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	beard dermatophytosis; dermatophytosis of beard; dermatophytosis of beard
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal