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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: Retinal Detachment (D012163)
..Starting node ..Retinal Nonattachment And Falciform Detachment (C566717)
Child Nodes:
Sister Nodes:
..Diverticulosis of Bowel, Hernia, and Retinal Detachment (C565619)
..Knobloch syndrome (C537209)
..Knobloch Syndrome Type II (C548030)
..Knobloch Syndrome Type III (C548031)
..Lattice Degeneration of Retina Leading to Retinal Detachment (C563633)
..Retinal Nonattachment And Falciform Detachment (C566717)
..Rhegmatogenous Retinal Detachment, Autosomal Dominant (C563710)
..Spondyloocular Syndrome, Autosomal Recessive (C565285)
..Stickler syndrome, type 1 (C537492)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9729
Name:	Retinal Nonattachment And Falciform Detachment
Definition:
Alternative IDs:
ParentIDs:	MESH:D012163
TreeNumbers:	C11.768.648/C566717
Synonyms:
Slim Mappings:	Eye disease
Reference:	MedGen: C566717 MeSH: C566717 OMIM: 180070; Genes:
Phenotypes
Disease Causing ClinVar Variants