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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: Vision Disorders (D014786)
..Starting node ..Photophobia (D020795)
Child Nodes:
........Ichthyosis follicularis atrichia photophobia syndrome (C536085)
........Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant (C567553)
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:	8915
Name:	Photophobia
Definition:	Abnormal sensitivity to light. This may occur as a manifestation of EYE DISEASES; MIGRAINE; SUBARACHNOID HEMORRHAGE; MENINGITIS; and other disorders. Photophobia may also occur in association with DEPRESSION and other MENTAL DISORDERS.
Alternative IDs:
ParentIDs:	MESH:D014786
TreeNumbers:	C10.597.751.941.661 \|C11.966.741 \|C23.888.592.763.941.661
Synonyms:	Light Sensitivities \|Light Sensitivity \|Photophobias \|Sensitivities, Light \|Sensitivity, Light
Slim Mappings:	Eye disease\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: D020795 MeSH: D020795 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants