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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: Agenesis of Corpus Callosum (D061085)
Parent Node: Cleft Lip (D002971)
Parent Node: Cleft Palate (D002972)
Parent Node: Encephalocele (D004677)
Parent Node: Meningocele (D008588)
..Starting node ..Sakoda Complex (C567055)
Child Nodes:
Sister Nodes:
..Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome (C565867)
..Lateral meningocele syndrome (C537878)
..Sacral Agenesis Syndrome (C566762)
..Sacral defect and anterior sacral meningocele (C537221)
..Sakoda Complex (C567055)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9945
Name:	Sakoda Complex
Definition:
Alternative IDs:
ParentIDs:	MESH:D002971\|MESH:D002972\|MESH:D004677\|MESH:D008588\|MESH:D061085
TreeNumbers:	C05.500.460.185/C567055 \|C05.660.207.540.460.185/C567055 \|C07.320.440.185/C567055 \|C07.465.409.225/C567055 \|C07.465.525.164/C567055 \|C07.465.525.185/C567055 \|C07.650.500.460.185/C567055 \|C07.650.525.164/C567055 \|C07.650.525.185/C567055 \|C10.500.034/C567055 \|C10.50
Synonyms:	Sakoda Spectrum \|Sphenoethmoidal Encephalomeningocele, Agenesis of the Corpus Callosum, and Cleft Lip/Palate
Slim Mappings:	Congenital abnormality\|Mouth disease\|Musculoskeletal disease\|Nervous system disease\|Pathology (anatomical condition)
Reference:	MedGen: C567055 MeSH: C567055 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants