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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: Muscular Atrophy (D009133)
..Starting node ..Sarcopenia (D055948)
Child Nodes:
Sister Nodes:
..Allan-Herndon-Dudley syndrome (C537047)
..Arnold Stickler Bourne syndrome (C537431)
..Facial Dysmorphism with Multiple Malformations (C565579)
..Furukawa Takagi Nakao syndrome (C538193)
..Lethal Congenital Contractural Syndrome 3 (C566961)
..MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT (OMIM:300354)
..Miyoshi Muscular Dystrophy 2 (C567646)
..Miyoshi Muscular Dystrophy 3 (C567645)
..Miyoshi myopathy (C537480)
..Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus (C562774)
..Muscular Atrophy, Malignant Neurogenic (C563559)
..Nathalie syndrome (C538342)
..Primrose syndrome (C536420)
..Sarcopenia (D055948)
..Thakker Donnai syndrome (C536503)
..Wieacker syndrome (C536703)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9992
Name:	Sarcopenia
Definition:	Progressive decline in muscle mass due to aging which results in decreased functional capacity of muscles.
Alternative IDs:
ParentIDs:	MESH:D009133
TreeNumbers:	C10.597.613.612.500 \|C23.300.070.500.500 \|C23.888.592.608.612.500
Synonyms:	Sarcopenias
Slim Mappings:	Nervous system disease\|Pathology (anatomical condition)\|Signs and symptoms
Reference:	MedGen: D055948 MeSH: D055948 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants