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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: Pain (D010146)
..Starting node ..Acute Pain (D059787)
Child Nodes:
Sister Nodes:
..Abdominal Pain (D015746) 4
..Acute Pain (D059787)
..Arthralgia (D018771) 1
..Back Pain (D001416) 2
..Breakthrough Pain (D059390)
..Chest Pain (D002637) 7
..Chronic Pain (D059350)
..Earache (D004433)
..Eye Pain (D058447)
..Facial Pain (D005157) 1
..Flank Pain (D021501)
..Glossalgia (D005926)
..Headache (D006261) 2
..Labor Pain (D048949)
..Levator syndrome (C535890)
..Mastodynia (D059373)
..Metatarsalgia (D037061)
..Musculoskeletal Pain (D059352) 2
..Neck Pain (D019547)
..Neuralgia (D009437) 6
..Neuropathy, Painful (C564945)
..Nociceptive Pain (D059226) 1
..Pain, Intractable (D010148)
..Pain, Postoperative (D010149) 1
..Pain, Referred (D053591)
..Paroxysmal Extreme Pain Disorder (C563475)
..Pelvic Pain (D017699) 4
..Shoulder Pain (D020069)
..Slit Ventricle Syndrome (D056124)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	243
Name:	Acute Pain
Definition:	Intensely discomforting, distressful, or agonizing sensation associated with trauma or disease, with well-defined location, character, and timing.
Alternative IDs:
ParentIDs:	MESH:D010146
TreeNumbers:	C10.597.617.088 \|C23.888.646.115
Synonyms:	Acute Pains \|Pain, Acute \|Pains, Acute
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D059787 MeSH: D059787 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants