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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: Pancytopenia (D010198)
..Starting node ..Sackey Sakati Aur syndrome (C537219)
Child Nodes:
Sister Nodes:
..Banti's syndrome (C537903)
..Fanconi like syndrome (C536855)
..Myelocerebellar Disorder (C563233)
..Pancytopenia and Occlusive Vascular Disease (C566836)
..Sackey Sakati Aur syndrome (C537219)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9932
Name:	Sackey Sakati Aur syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D000015\|MESH:D010198
TreeNumbers:	C15.378.700/C537219 \|C16.131.077/C537219
Synonyms:	Aur syndrome \|Multiple dysmorphic features and pancytopenia \|Pancytopenia multiple congenital anomalies
Slim Mappings:	Blood disease\|Congenital abnormality
Reference:	MedGen: C537219 MeSH: C537219 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants