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: dermatitis (MONDO:0002406)
Parent Node: disease of pilosebaceous unit (MONDO:0002917)
..Starting node ..folliculitis ()
Child Nodes:
........acne keloid ()
........Demodex folliculitis ()
........eosinophilic pustular folliculitis ()
........keratosis follicularis spinulosa decalvans ()
Sister Nodes:
..catatrichy ()
..folliculitis ()
..hair anomaly ()
..hair follicle neoplasm ()
..hypotrichosis ()
..Katsantoni-Papadakou-Lagoyanni syndrome ()
..piedra ()
..sebaceous gland disease ()
..trichostasis spinulosa ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6552
Name:	folliculitis
Definition:	Inflammation of the hair follicles. Causes include excessive perspiration, skin infections, and skin wounds.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	dermatitis of hair follicle; hair follicle dermatitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal