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: lacrimal apparatus disease (MONDO:0001854)
..Starting node ..excessive tearing ()
Child Nodes:
........epiphora due to excess lacrimation ()
........epiphora due to insufficient drainage ()
Sister Nodes:
..acute inflammation of lacrimal passage ()
..anomaly of the secretory and excretory apparatus of the lacrimal system ()
..chronic inflammation of lacrimal passage ()
..disorder of lacrimal gland ()
..dry eye syndrome ()
..eversion of lacrimal punctum ()
..excessive tearing ()
..excretory apparatus of the lacrimal system anomaly ()
..IgG4-related dacryoadenitis and sialadenitis ()
..lacrimal passage granuloma ()
..lacrimal system cancer ()
..nasolacrimal duct disease ()
..primary lacrimal atrophy ()
..secretory apparatus of the lacrimal system anomaly ()
..stenosis of lacrimal passage ()
..stenosis of lacrimal punctum ()
..stenosis of lacrimal sac ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1793
Name:	excessive tearing
Definition:	Diseases of the lacrimal apparatus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	apparatus disease, lacrimal; apparatus diseases, lacrimal; disease, lacrimal apparatus; diseases, lacrimal apparatus; epiphora; excessive tear production; lacrimal apparatus disease; watering eye
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: PPARG;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal