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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: Mouth Diseases (D009059)
..Starting node ..Leukoedema, Oral (D007967)
Child Nodes:
Sister Nodes:
..Behcet Syndrome (D001528)
..Bell Palsy (D020330)
..Burning Mouth Syndrome (D002054) 2
..Candidiasis, Oral (D002180)
..Dry Socket (D004368)
..Facial Hemiatrophy (D005150)
..Facial Neuralgia (D005156)
..Facial Paralysis (D005158) 6
..Focal Epithelial Hyperplasia (D017573) 1
..Granulomatosis, Orofacial (D051261)
..Hemifacial Spasm (D019569) 1
..Leukoedema, Oral (D007967)
..Lichen Planus, Oral (D017676)
..Lip Diseases (D008047) 67
..Ludwig's Angina (D008158)
..Melkersson-Rosenthal Syndrome (D008556)
..Mouth Abnormalities (D009056) 144
..Mouth Neoplasms (D009062) 14
..Mouth, Edentulous (D009066) 2
..Mucositis (D052016)
..Noma (D009625) 1
..Oral Fistula (D016155) 3
..Oral Hemorrhage (D006472) 2
..Oral Manifestations (D009912) 3
..Oral Submucous Fibrosis (D009914)
..Oral Ulcer (D019226)
..Peri-Implantitis (D057873)
..Periodontal Diseases (D010510) 54
..Ranula (D011900)
..Salivary Gland Diseases (D012466) 29
..Stomatitis (D013280) 6
..Tongue Diseases (D014060) 15
..Tuberculosis, Oral (D014393)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6388
Name:	Leukoedema, Oral
Definition:	A disorder of the buccal mucosa resembling early leukoplakia, characterized by the presence of filmy opalescence of the mucosa in the early stages to a whitish gray cast with a coarsely wrinkled surface in the later stages, associated with intracellular edema of the spinous or malpighian layer. (Dorland, 27th ed)
Alternative IDs:
ParentIDs:	MESH:D009059
TreeNumbers:	C07.465.385
Synonyms:	Leukoedemas, Oral \|Oral Leukoedema \|Oral Leukoedemas
Slim Mappings:	Mouth disease
Reference:	MedGen: D007967 MeSH: D007967 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants