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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: Metabolic Diseases (D008659)
Parent Node: Nutrition Disorders (D009748)
..Starting node ..Wasting Syndrome (D019282)
Child Nodes:
........HIV Wasting Syndrome (D019247)
Sister Nodes:
..Child Nutrition Disorders (D015362)
..Hypervitaminosis A (D006986)
..Infant Nutrition Disorders (D007228) 1
..Malnutrition (D044342) 69
..Overnutrition (D044343) 43
..Wasting Syndrome (D019282) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11708
Name:	Wasting Syndrome
Definition:	A condition of involuntary weight loss of greater then 10% of baseline body weight. It is characterized by atrophy of muscles and depletion of lean body mass. Wasting is a sign of MALNUTRITION as a result of inadequate dietary intake, malabsorption, or hypermetabolism.
Alternative IDs:
ParentIDs:	MESH:D008659\|MESH:D009748
TreeNumbers:	C18.452.915 \|C18.654.940
Synonyms:	Wasting Disease \|Wasting Diseases \|Wasting Syndromes
Slim Mappings:	Metabolic disease\|Nutrition disorder
Reference:	MedGen: D019282 MeSH: D019282 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants