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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: Chromosome Deletion (D002872)
Parent Node: WAGR Syndrome (D017624)
..Starting node ..Chromosome 11p Deletion Syndrome (C541598)
Child Nodes:
Sister Nodes:
..Chromosome 11p Deletion Syndrome (C541598)
..Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome (C567292)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	2189
Name:	Chromosome 11p Deletion Syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D002872\|MESH:D017624
TreeNumbers:	C04.557.435.595.950/C541598 \|C04.588.945.947.535.585.950/C541598 \|C04.700.635.950/C541598 \|C10.597.606.643.969/C541598 \|C11.250.060.950/C541598 \|C11.270.060.950/C541598 \|C11.941.375.060.950/C541598 \|C12.706.316.096.875/C541598 \|C12.758.820.750.585.950/C541598 \|C1
Synonyms:	11p Deletion Syndrome
Slim Mappings:	Cancer\|Congenital abnormality\|Endocrine system disease\|Eye disease\|Genetic disease (inborn)\|Nervous system disease\|Pathology (process)\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C541598 MeSH: C541598 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants