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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Ossification, Heterotopic (D009999)

       Child Nodes:
........expandDesbuquois syndrome (C535943)
........expandEagle syndrome (C538010)
........expandLeri pleonosteosis (C537118)
........expandOsseous Heteroplasia, Progressive (C562735)
........expandOssification of Posterior Longitudinal Ligament (D017887) Child1
........expandSuperior Transverse Scapular Ligament, Calcification Of, Familial (C566638)



 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:8363
Name:Ossification, Heterotopic
Definition:The development of bony substance in normally soft structures.
Alternative IDs:
ParentIDs:MESH:D010335
TreeNumbers:C23.550.751
Synonyms:Ectopic Ossification |Heterotopic Ossification |Ossification, Ectopic |Ossification, Pathologic |Ossification, Pathological |Pathological Ossification |Pathologic Ossification
Slim Mappings:Pathology (process)
Reference: MedGen: D009999
MeSH: D009999
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants