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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: Campomelic Dysplasia (D055036)
Parent Node: Lymphocele (D008210)
Parent Node: Multicystic Dysplastic Kidney (D021782)
..Starting node ..Campomelia Cumming type (C537966)
Child Nodes:
Sister Nodes:
..Campomelia Cumming type (C537966)
..Multicystic renal dysplasia, bilateral (C537373)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1581
Name:	Campomelia Cumming type
Definition:
Alternative IDs:
ParentIDs:	MESH:D008210\|MESH:D021782\|MESH:D055036
TreeNumbers:	C04.182.430/C537966 \|C05.660.142/C537966 \|C12.706.629/C537966 \|C12.777.419.403.750/C537966 \|C13.351.875.558/C537966 \|C13.351.968.419.403.750/C537966 \|C15.604.510/C537966 \|C16.131.621.142/C537966 \|C16.131.939.629/C537966
Synonyms:	Campomelia, Cumming Type \|Cervical lymphocele with bowed long bones \|Cumming syndrome
Slim Mappings:	Cancer\|Congenital abnormality\|Lymphatic disease\|Musculoskeletal disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C537966 MeSH: C537966 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants