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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: Abnormalities, Multiple (D000015)
Parent Node: Heart Defects, Congenital (D006330)
Parent Node: Jaw Abnormalities (D007569)
Parent Node: Mouth Abnormalities (D009056)
Parent Node: Pregnancy in Diabetics (D011254)
..Starting node ..Verloove-Vanhorick Brubakk syndrome (C536541)
Child Nodes:
Sister Nodes:
..Fetal Macrosomia (D005320) 4
..Verloove-Vanhorick Brubakk syndrome (C536541)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11581
Name:	Verloove-Vanhorick Brubakk syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D000015\|MESH:D006330\|MESH:D007569\|MESH:D009056\|MESH:D011254
TreeNumbers:	C05.500.460/C536541 \|C05.660.207.540.460/C536541 \|C07.320.440/C536541 \|C07.465.525/C536541 \|C07.650.500.460/C536541 \|C07.650.525/C536541 \|C13.703.726/C536541 \|C14.240.400/C536541 \|C14.280.400/C536541 \|C16.131.077/C536541 \|C16.131.240.400/C536541 \|C16.131.621.207.54
Synonyms:	Cleft Limb Heart Malformation Syndrome \|Cleft-Limb-Heart Malformation Syndrome \|Verloove Vanhorick Brubakk syndrome
Slim Mappings:	Cardiovascular disease\|Congenital abnormality\|Mouth disease\|Musculoskeletal disease\|Pregnancy complication
Reference:	MedGen: C536541 MeSH: C536541 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants