Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
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Neoplasms (D009369)
Parent Node:
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Pathological Conditions, Anatomical (D020763)
..Starting node
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Cysts (D003560)

       Child Nodes:
........expandAplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts (C566997)
........expandArachnoid Cysts (D016080) Child6
........expandBone Cysts (D001845) Child11
........expandBranchioma (D001935)
........expandBreast Cyst (D047688) Child1
........expandBronchogenic Cyst (D001994)
........expandChalazion (D017043)
........expandCholedochal Cyst (D015529) Child2
........expandColloid Cysts (D056364) Child1
........expandCystic medial necrosis of aorta (C536230)
........expandDermoid Cyst (D003884) Child5
........expandEctodermal dysplasia adrenal cyst (C538015)
........expandEpidermal Cyst (D004814) Child2
........expandEsophageal Cyst (D004934)
........expandFollicular Cyst (D005497) Child2
........expandGanglion Cysts (D045888)
........expandLeukoencephalopathy, Cystic, Without Megalencephaly (C567845)
........expandLymphocele (D008210) Child1
........expandMediastinal Cyst (D008476)
........expandMegalencephalic leukoencephalopathy with subcortical cysts (C536141)
........expandMesenteric Cyst (D008639)
........expandMicrophthalmia associated with colobomatous cyst (C537463)
........expandMucocele (D009078)
........expandOvarian Cysts (D010048) Child5
........expandPancreatic Cyst (D010181) Child2
........expandParovarian Cyst (D010310)
........expandPilonidal Sinus (D010864)
........expandPolycystic liver disease (C536330)
........expandRanula (D011900)
........expandSener syndrome (C537579)
........expandSpermatocele (D013088)
........expandSynovial Cyst (D013581) Child1
........expandTarlov Cysts (D052958)
........expandThyroglossal Cyst (D013955) Child1
........expandUrachal Cyst (D014496) Child1
........expandVan der Woude syndrome (C536528) Child1



 Sister Nodes: 
..expandAccessory Atrioventricular Bundle (D058606)
..expandAgenesis of Corpus Callosum (D061085) Child59
..expandAirway Remodeling (D056151)
..expandAlopecia (D000505) Child61
..expandAtrial Remodeling (D064752)
..expandAtrophy (D001284) Child18
..expandBlister (D001768) Child3
..expandCalculi (D002137) Child15
..expandChoristoma (D002828) Child2
..expandConstriction, Pathologic (D003251) Child9
..expandCysts (D003560) Child78
..expandDilatation, Pathologic (D004108)
..expandDiverticulum (D004240) Child7
..expandFacial Asymmetry (D005146) Child8
..expandFistula (D005402) Child34
..expandHernia (D006547) Child73
..expandHypertrophy (D006984) Child62
..expandLeg Length Inequality (D007870)
..expandLeukoplakia (D007971) Child2
..expandNails, Malformed (D009264) Child44
..expandPlaque, Amyloid (D058225) Child1
..expandPlaque, Atherosclerotic (D058226)
..expandPolyps (D011127) Child7
..expandProlapse (D011391) Child5
..expandRupture, Spontaneous (D012422) Child1
..expandTorsion Abnormality (D014102) Child13
..expandVascular Remodeling (D066253)
..expandVentricular Remodeling (D020257)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:2951
Name:Cysts
Definition:Any fluid-filled closed cavity or sac that is lined by an EPITHELIUM. Cysts can be of normal, abnormal, non-neoplastic, or neoplastic tissues.
Alternative IDs:
ParentIDs:MESH:D009369|MESH:D020763
TreeNumbers:C04.182 |C23.300.306
Synonyms:Cyst
Slim Mappings:Cancer|Pathology (anatomical condition)
Reference: MedGen: D003560
MeSH: D003560
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants