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: fungal infectious disease (MONDO:0002041)
Parent Node: integumentary system disease (MONDO:0002051)
..Starting node ..cutaneous mycosis ()
Child Nodes:
........cutaneous basidiobolomycosis ()
........cutaneous candidiasis ()
........dermatomycosis ()
........otomycosis ()
........subcutaneous mycosis ()
........superficial mycosis ()
........tinea favosa ()
Sister Nodes:
..Bartholin duct cyst ()
..Bartholin gland neoplasm ()
..benign mammary dysplasia ()
..breast fibrocystic disease ()
..cervical aortic arch ()
..corneal disease ()
..cutaneous mycosis ()
..demodicidosis ()
..dermis disease ()
..disease of pilosebaceous unit ()
..integumentary system benign neoplasm ()
..integumentary system cancer ()
..keratinization disease ()
..lip disease ()
..nail disease ()
..neoplasm of aortic body ()
..panniculitis ()
..pseudoxanthoma elasticum (inherited or acquired) ()
..skin appendage disease ()
..skin disease ()
..subcutaneous tissue disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	254
Name:	cutaneous mycosis
Definition:	A mycosis that involves the integument and its appendages, including hair and nails. Infection may involve the stratum corneum or deeper layers of the epidermis.
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Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: ARHGAP31;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal