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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: Migraine Disorders (D008881)
Parent Node: Perceptual Disorders (D010468)
Parent Node: Vision Disorders (D014786)
..Starting node ..Alice in Wonderland Syndrome (D062026)
Child Nodes:
Sister Nodes:
..Alice in Wonderland Syndrome (D062026)
..Amblyopia (D000550) 2
..Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction (C563394)
..Blindness (D001766) 39
..Color Vision Defects (D003117) 11
..Creutzfeldt-Jakob Disease, Heidenhain Variant (C566981)
..Diplopia (D004172)
..Enhanced S-Cone Syndrome (C564835)
..Hemianopsia (D006423)
..Night Blindness (D009755) 14
..Photophobia (D020795) 2
..Scotoma (D012607) 1
..Siegler Brewer Carey syndrome (C537335)
..SPATIAL VISUALIZATION, APTITUDE FOR (OMIM:313000)
..Susac Syndrome (D055955)
..Vision, Low (D015354)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	430
Name:	Alice in Wonderland Syndrome
Definition:	Neurological condition characterized by disturbances in VISUAL PERCEPTION, most often of BODY SCHEMA, TIME PERCEPTION and HALLUCINATIONS. It is associated with MIGRAINE, infections (e.g., INFECTIOUS MONONUCLEOSIS), FEVER, EPILEPSY, and other neurological and psychiatric disorders.
Alternative IDs:
ParentIDs:	MESH:D008881\|MESH:D010468\|MESH:D014786
TreeNumbers:	C10.228.140.546.399.750.124 \|C10.597.606.762.150 \|C10.597.751.941.036 \|C23.888.592.604.764.150 \|C23.888.592.763.941.036
Synonyms:
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D062026 MeSH: D062026 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants