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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Lymphoproliferative Disorders (D008232)
Parent Node:
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Pathologic Processes (D010335)
..Starting node
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Granuloma (D006099)

       Child Nodes:
........expandAngiolymphoid Hyperplasia with Eosinophilia (D000796)
........expandChurg-Strauss Syndrome (D015267)
........expandEosinophilic Granuloma (D004803)
........expandGranuloma Annulare (D016460)
........expandGranuloma, Foreign-Body (D015745)
........expandGranuloma, Giant Cell (D006101) Child3
........expandGranuloma, Plasma Cell (D006104)
........expandGranuloma, Pyogenic (D017789)
........expandGranuloma, Respiratory Tract (D015769) Child1
........expandGranulomas, congenital cerebral (C537294)
........expandNecrobiotic Xanthogranuloma (D058252)
........expandXanthogranulomatous cholecystitis (C536762)
........expandXanthogranulomatous sialadenitis (C536763)



 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:4785
Name:Granuloma
Definition:A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents.
Alternative IDs:
ParentIDs:MESH:D008232|MESH:D010335
TreeNumbers:C15.604.515.292 |C23.550.382
Synonyms:Granulomas
Slim Mappings:Lymphatic disease|Pathology (process)
Reference: MedGen: D006099
MeSH: D006099
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants