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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 ..Facial Pain (D005157)
Child Nodes:
........Toothache (D014098)
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:	4082
Name:	Facial Pain
Definition:	Pain in the facial region including orofacial pain and craniofacial pain. Associated conditions include local inflammatory and neoplastic disorders and neuralgic syndromes involving the trigeminal, facial, and glossopharyngeal nerves. Conditions which feature recurrent or persistent facial pain as the primary manifestation of disease are referred to as FACIAL PAIN SYNDROMES.
Alternative IDs:
ParentIDs:	MESH:D010146
TreeNumbers:	C10.597.617.364 \|C23.888.592.612.330 \|C23.888.646.429
Synonyms:	Craniofacial Pain \|Face Pain \|Facial Pain, Neuralgic \|Myofacial Pain \|Neuralgic Facial Pain \|Orofacial Pain \|Pain, Craniofacial \|Pain, Face \|Pain, Facial \|Pain, Myofacial \|Pain, Neuralgic Facial \|Pain, Orofacial
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D005157 MeSH: D005157 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants