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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: Cataract (D002386)
Parent Node: Corneal Diseases (D003316)
..Starting node ..Cataract microcornea syndrome (C538287)
Child Nodes:
Sister Nodes:
..Arnold Stickler Bourne syndrome (C537431)
..Cataract microcornea syndrome (C538287)
..Cornea Plana 1 (C565158)
..Cornea Plana 2 (C565677)
..Corneal Dystrophies, Hereditary (D003317) 61
..Corneal Edema (D015715)
..Corneal Endothelial Cell Loss (D055954)
..Corneal hypesthesia, familial (C536440)
..Corneal Injuries (D065306) 1
..Corneal Neovascularization (D016510)
..Corneal Opacity (D003318) 10
..Corneal Wavefront Aberration (D057108)
..Dermoids of cornea (C535376)
..Iridocorneal Endothelial Syndrome (D057129)
..Keratitis (D007634) 14
..Keratoconus (D007640) 9
..Macrophthalmia, Colobomatous, with Microcornea (C566533)
..Microspherophakia (C563255)
..Neuhauser syndrome (C536143)
..Ramos Arroyo Clark syndrome (C535286)
..Ring dermoid of cornea (C535684)
..Sclerocornea (C565209)
..Sclerocornea, Autosomal Dominant (C566692)
..Stern Lubinsky Durrie syndrome (C537488)
..Trachoma (D014141)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1848
Name:	Cataract microcornea syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D002386\|MESH:D003316
TreeNumbers:	C11.204/C538287 \|C11.510.245/C538287
Synonyms:	Cataract-Microcornea Syndrome \|Microcornea cataract syndrome \|Microcornea-Cataract Syndrome
Slim Mappings:	Eye disease
Reference:	MedGen: C538287 MeSH: C538287 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants