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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: Keratoconus (D007640)
..Starting node ..Noninflammatory corneal thinning (C531720)
Child Nodes:
Sister Nodes:
..Keratoconus 1 (C563649)
..Keratoconus 2 (C563827)
..Keratoconus 3 (C563900)
..Keratoconus 4 (C563752)
..Keratoconus And Congenital Hip Dysplasia (C565456)
..Keratoconus posticus circumscriptus (C536151)
..Keratoconus Posticus Circumscriptus with Associated Malformations (C565455)
..Mental retardation, keratoconus, febrile seizures, and sinoatrial block (C537452)
..Noninflammatory corneal thinning (C531720)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8103
Name:	Noninflammatory corneal thinning
Definition:
Alternative IDs:
ParentIDs:	MESH:D007640
TreeNumbers:	C11.204.627/C531720
Synonyms:
Slim Mappings:	Eye disease
Reference:	MedGen: C531720 MeSH: C531720 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants