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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: Cerebral Palsy (D002547)
..Starting node ..Cerebral palsy, spastic, diplegic (C537945)
Child Nodes:
Sister Nodes:
..Cerebral Palsy, Ataxic, Autosomal Recessive (C562856)
..Cerebral Palsy, Spastic Quadriplegic, 1 (C567853)
..Cerebral Palsy, Spastic Quadriplegic, 2 (C567867)
..Cerebral palsy, spastic, diplegic (C537945)
..Dysmyelination With Jaundice (C565610)
..Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation (C565587)
..Neuhauser syndrome (C536143)
..Paine syndrome (C538101)
..Renpenning syndrome 1 (C537761)
..Spastic Paraplegia-50, Autosomal Recessive (C567858)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1949
Name:	Cerebral palsy, spastic, diplegic
Definition:
Alternative IDs:
ParentIDs:	MESH:D002547
TreeNumbers:	C10.228.140.140.254/C537945
Synonyms:	Spastic diplegia cerebral palsy
Slim Mappings:	Nervous system disease
Reference:	MedGen: C537945 MeSH: C537945 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants