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: immune system disease (MONDO:0005046)
Parent Node: opportunistic mycosis (MONDO:0002312)
..Starting node ..geotrichosis ()
Child Nodes:
Sister Nodes:
..aspergillosis ()
..candidiasis ()
..cryptococcosis ()
..fusariosis ()
..geotrichosis ()
..hyalohyphomycosis ()
..maple bark strippers' lung ()
..microsporidiosis ()
..opportunistic systemic mycosis ()
..phaeohyphomycosis ()
..pneumocystosis ()
..Zygomycosis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5772
Name:	geotrichosis
Definition:	Infection due to the fungus Geotrichum.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal