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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: Anemia, Aplastic (D000741)
Parent Node: Leukemia (D007938)
..Starting node ..WT limb blood syndrome (C536751)
Child Nodes:
Sister Nodes:
..Enzootic Bovine Leukosis (D016583)
..Leukemia, Acute, X-Linked (C564112)
..Leukemia, Experimental (D007942) 4
..Leukemia, Feline (D016582)
..Leukemia, Hairy Cell (D007943)
..Leukemia, Lymphoid (D007945) 14
..Leukemia, Mast-Cell (D007946)
..Leukemia, Myeloid (D007951) 30
..Leukemia, Plasma Cell (D007952)
..Leukemia, Radiation-Induced (D007953)
..WT limb blood syndrome (C536751)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11802
Name:	WT limb blood syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D000015\|MESH:D000741\|MESH:D007938
TreeNumbers:	C04.557.337/C536751 \|C15.378.071.085/C536751 \|C15.378.190.196/C536751 \|C16.131.077/C536751
Synonyms:	Radial-ulnar hypoplasia with bone marrow failure and/or leukemia \|WT Limb-Blood Syndrome
Slim Mappings:	Blood disease\|Cancer\|Congenital abnormality
Reference:	MedGen: C536751 MeSH: C536751 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants