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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

Disease Browser
Parent Node: Pupil Disorders (D011681)
..Starting node ..Miosis (D015877)
Child Nodes:
........Ataxia, Spastic, with Congenital Miosis (C566247)
........Horner Syndrome (D006732) 1
........Ophthalmoplegia Totalis with Ptosis and Miosis (C564927)
........Stormorken Syndrome (C566108)
Sister Nodes:
..Anisocoria (D015875)
..Congenital Corneal Opacities, Cornea Guttata, and Corectopia (C563921)
..Ectopia Lentis with Ectopia of Pupil (C563268)
..Ectopia pupillae (C536185)
..McPherson Robertson Cammarano syndrome (C538161)
..Microcoria, congenital (C537550)
..Microphthalmia, Isolated, With Corectopia (C563581)
..Miosis (D015877) 5
..Mydriasis (D015878) 1
..Pierson syndrome (C537185)
..Ptosis, Strabismus, And Ectopic Pupils (C566736)
..Tonic Pupil (D015845) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7300
Name:	Miosis
Definition:	Pupillary constriction. This may result from congenital absence of the dilatator pupillary muscle, defective sympathetic innervation, or irritation of the CONJUNCTIVA or CORNEA.
Alternative IDs:
ParentIDs:	MESH:D011681
TreeNumbers:	C10.597.690.362 \|C11.710.528 \|C23.888.592.708.362
Synonyms:	Constricted Pupil \|Constricted Pupils \|Mioses \|Mioses, Persistent \|Mioses, Pupillary \|Miosis, Persistent \|Miosis, Pupillary \|Persistent Mioses \|Persistent Miosis \|Pupil, Constricted \|Pupillary Mioses \|Pupillary Miosis \|Pupils, Constricted \|Pupil, Small \|Pupils, Small \|
Slim Mappings:	Eye disease\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: D015877 MeSH: D015877 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants