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
..expand
Sclerosis (D012598)

       Child Nodes:
........expandMediastinal Fibrosis (C536136)
........expandMesangial sclerosis, diffuse (C537346)
........expandMesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities (C565405)
........expandOsteosclerosis with ichthyosis and premature ovarian failure (C536064)
........expandPoikiloderma, Hereditary Sclerosing (C562824)
........expandScleroatonic muscular dystrophy (C537521)
........expandSclerosing bone dysplasia mental retardation (C537523)
........expandSclerosing lymphocytic lobulitis (C537524)



 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:10066
Name:Sclerosis
Definition:A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve.
Alternative IDs:
ParentIDs:MESH:D010335
TreeNumbers:C23.550.823
Synonyms:Scleroses
Slim Mappings:Pathology (process)
Reference: MedGen: D012598
MeSH: D012598
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants