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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: Facial Nerve Diseases (D005155)
Parent Node: Mouth Diseases (D009059)
..Starting node ..Facial Hemiatrophy (D005150)
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:	4074
Name:	Facial Hemiatrophy
Definition:	A syndrome characterized by slowly progressive unilateral atrophy of facial subcutaneous fat, muscle tissue, skin, cartilage, and bone. The condition typically progresses over a period of 2-10 years and then stabilizes.
Alternative IDs:
ParentIDs:	MESH:D005155\|MESH:D009059
TreeNumbers:	C07.465.284 \|C10.292.300.375
Synonyms:	Atrophies, Hemifacial \|Atrophies, Progressive Hemifacial \|Atrophy, Hemifacial \|Atrophy, Progressive Hemifacial \|Atrophy, Romberg Hemi-Facial \|Disease, Parry-Romberg \|Disease, Romberg \|Disease, Romberg's \|Facial Hemiatrophies \|Facial Hemiatrophies, Progressive \|Fac
Slim Mappings:	Mouth disease\|Nervous system disease
Reference:	MedGen: D005150 MeSH: D005150 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants