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
Hemorrhage (D006470)

       Child Nodes:
........expandBleeding Disorder Due To P2rx1 Defect (C576084)
........expandBLEEDING DISORDER, PLATELET-TYPE, 8 (OMIM:609821)
........expandBlood Loss, Surgical (D016063)
........expandCircumvallate Placenta Syndrome (C565847)
........expandEcchymosis (D004438)
........expandEpistaxis (D004844) Child1
........expandExsanguination (D058734)
........expandEye Hemorrhage (D005130) Child6
........expandGastrointestinal Hemorrhage (D006471) Child3
........expandHemarthrosis (D006395)
........expandHematocele (D006398)
........expandHematoma (D006406) Child7
........expandHematuria (D006417) Child2
........expandHemobilia (D006431)
........expandHemoperitoneum (D006465)
........expandHemoptysis (D006469)
........expandHemothorax (D006491) Child1
........expandIntracranial Hemorrhages (D020300) Child24
........expandOral Hemorrhage (D006472) Child2
........expandPostoperative Hemorrhage (D019106) Child1
........expandPurpura (D011693) Child15
........expandRapidly progressive glomerulonephritis with pulmonary hemorrhage (C538458)
........expandRetrobulbar Hemorrhage (D019315)
........expandShock, Hemorrhagic (D012771)
........expandUterine Hemorrhage (D014592) Child3



 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:5049
Name:Hemorrhage
Definition:Bleeding or escape of blood from a vessel.
Alternative IDs:
ParentIDs:MESH:D010335
TreeNumbers:C23.550.414
Synonyms:Bleeding |Hemorrhages
Slim Mappings:Pathology (process)
Reference: MedGen: D006470
MeSH: D006470
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants