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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: Diseases (C)
Parent Node: Van der Woude syndrome (C536528)
..Starting node ..VAN DER WOUDE SYNDROME 1, MODIFIER OF (OMIM:604547)
Child Nodes:
Sister Nodes:
..VAN DER WOUDE SYNDROME 1, MODIFIER OF (OMIM:604547)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11516
Name:	VAN DER WOUDE SYNDROME 1, MODIFIER OF
Definition:
Alternative IDs:
ParentIDs:	MESH:C536528
TreeNumbers:	C04.182/C536528/604547 \|C05.500.460.185/C536528/604547 \|C05.660.207.540.460.185/C536528/604547 \|C07.320.440.185/C536528/604547 \|C07.465.409.225/C536528/604547 \|C07.465.525.164/C536528/604547 \|C07.465.525.185/C536528/604547 \|C07.650.500.460.185/C536528/604547 \|C0
Synonyms:	VWSM
Slim Mappings:	Cancer\|Congenital abnormality\|Mouth disease\|Musculoskeletal disease\|Pathology (anatomical condition)
Reference:	MedGen: 604547 MeSH: 604547 OMIM: 604547; Genes:
Phenotypes
Disease Causing ClinVar Variants