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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Pathologic Processes (D010335)
..Starting node
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Fibrosis (D005355)

       Child Nodes:
........expandCicatrix (D002921) Child5
........expandFibrosis Of Extraocular Muscles, Congenital, 2 (C566587)
........expandFibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement (C567572)
........expandFibrosis of Extraocular Muscles, Congenital, 3B (C567739)
........expandFibrosis of Extraocular Muscles, Congenital, 3C (C567666)
........expandFibrosis of Extraocular Muscles, Congenital, with Synergistic Divergence (C566508)
........expandNephrogenic Fibrosing Dermopathy (D054989)
........expandPeritoneal Fibrosis (D056627)
........expandRetroperitoneal Fibrosis (D012185) Child1
........expandTukel syndrome (C536925)



 Sister Nodes: 
..expandAcantholysis (D000051) Child1
..expandArrhythmias, Cardiac (D001145) Child112
..expandAscites (D001201)
..expandAtrial Remodeling (D064752)
..expandAzotemia (D053099)
..expandCardiotoxicity (D066126)
..expandChannelopathies (D053447) Child1
..expandChromosome Aberrations (D002869) Child271
..expandDeath (D003643) Child27
..expandDehydration (D003681)
..expandDelayed Graft Function (D051799)
..expandDisease (D004194) Child1
..expandDisease Attributes (D020969) Child171
..expandDysbiosis (D064806)
..expandEmphysema (D004646) Child6
..expandExtravasation of Diagnostic and Therapeutic Materials (D005119)
..expandFemoracetabular Impingement (D057925)
..expandFibrosis (D005355) Child16
..expandGenomic Instability (D042822) Child5
..expandGliosis (D005911) Child1
..expandGranuloma (D006099) Child17
..expandGranulomatosis, Orofacial (D051261)
..expandGrowth Disorders (D006130) Child191
..expandHemolysis (D006461) Child2
..expandHemorrhage (D006470) Child84
..expandHyperammonemia (D022124) Child3
..expandHyperamylasemia (D034321)
..expandHyperbilirubinemia (D006932) Child13
..expandHyperplasia (D006965) Child4
..expandHyperuricemia (D033461) Child8
..expandHypovolemia (D020896)
..expandInflammation (D007249) Child52
..expandIntraoperative Complications (D007431) Child15
..expandIschemia (D007511) Child3
..expandLeukoaraiosis (D049292)
..expandLeukocytosis (D007964) Child6
..expandLithiasis (D020347)
..expandMalacoplakia (D008287) Child1
..expandMenstruation Disturbances (D008599) Child10
..expandMetaplasia (D008679) Child4
..expandMuscle Weakness (D018908) Child5
..expandNecrosis (D009336) Child12
..expandNeointima (D058426)
..expandNeoplastic Processes (D009385) Child18
..expandNerve Degeneration (D009410) Child7
..expandOchronosis (D009794) Child2
..expandOssification, Heterotopic (D009999) Child7
..expandPolydipsia (D059606) Child1
..expandPostoperative Complications (D011183) Child42
..expandProtein Aggregation, Pathological (D066263)
..expandRespiratory Aspiration (D053120) Child1
..expandRetropneumoperitoneum (D012188)
..expandSclerosis (D012598) Child8
..expandShock (D012769) Child18
..expandTeratogenesis (D064793)
..expandUlcer (D014456) Child1
..expandVascular Remodeling (D066253)
..expandYang Deficiency (D016711)
..expandYin Deficiency (D016710)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:4291
Name:Fibrosis
Definition:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury.
Alternative IDs:
ParentIDs:MESH:D010335
TreeNumbers:C23.550.355
Synonyms:Cirrhosis |Fibroses
Slim Mappings:Pathology (process)
Reference: MedGen: D005355
MeSH: D005355
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants