Disease Browser
Parent Node: Pathological Conditions, Anatomical (D020763) ..Starting node .. Atrophy (D001284) Child Nodes:
........MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY (OMIM:613668) ........Muscular Atrophy (D009133) 16 Sister Nodes: ..Accessory Atrioventricular Bundle (D058606) ..Agenesis of Corpus Callosum (D061085) 59 ..Airway Remodeling (D056151) ..Alopecia (D000505) 61 ..Atrial Remodeling (D064752) ..Atrophy (D001284) 18 ..Blister (D001768) 3 ..Calculi (D002137) 15 ..Choristoma (D002828) 2 ..Constriction, Pathologic (D003251) 9 ..Cysts (D003560) 78 ..Dilatation, Pathologic (D004108) ..Diverticulum (D004240) 7 ..Facial Asymmetry (D005146) 8 ..Fistula (D005402) 34 ..Hernia (D006547) 73 ..Hypertrophy (D006984) 62 ..Leg Length Inequality (D007870) ..Leukoplakia (D007971) 2 ..Nails, Malformed (D009264) 44 ..Plaque, Amyloid (D058225) 1 ..Plaque, Atherosclerotic (D058226) ..Polyps (D011127) 7 ..Prolapse (D011391) 5 ..Rupture, Spontaneous (D012422) 1 ..Torsion Abnormality (D014102) 13 ..Vascular Remodeling (D066253) ..Ventricular Remodeling (D020257) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 1049
Name: Atrophy
Definition: Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes.
Alternative IDs:
ParentIDs: MESH:D020763
TreeNumbers: C23.300.070
Synonyms: Atrophies
Slim Mappings: Pathology (anatomical condition)
Reference:
MedGen: D001284
MeSH: D001284
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants