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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Joint Diseases (D007592)
..Starting node
..expand
Ankylosis (D000844)

       Child Nodes:
........expandPiussan Lenaerts Mathieu syndrome (C537511)
........expandPseudoarthrogryposis (C566753)
........expandSpondylitis, Ankylosing (D013167) Child2
........expandSTAPES ANKYLOSIS WITH BROAD THUMB AND TOES (OMIM:184460)
........expandSymphalangism of Toes (C566101)
........expandSymphalangism, Distal (C566099) Child1
........expandTemporomandibular ankylosis (C536957)



 Sister Nodes: 
..expandAnkylosis (D000844) Child10
..expandArthralgia (D018771) Child1
..expandArthritis (D001168) Child57
..expandArthrogryposis (D001176) Child55
..expandArthropathy, Neurogenic (D001177) Child3
..expandBorrone Di Rocco Crovato syndrome (C536577)
..expandBrachydactylous dwarfism Mseleni type (C537086)
..expandBursitis (D002062) Child1
..expandCalcification of Joints and Arteries (C565891)
..expandChondromatosis, Synovial (D015838) Child1
..expandContracture (D003286) Child41
..expandCoracoclavicular Joint, Anomalous (C565161)
..expandCushing's symphalangism (C536223)
..expandDwarfism stiff joint ocular abnormalities (C535724)
..expandFemoracetabular Impingement (D057925)
..expandFlynn Aird syndrome (C537066)
..expandGEMSS syndrome (C537679)
..expandGrowth mental deficiency syndrome of Myhre (C537620)
..expandHallux Limitus (D020857)
..expandHallux Rigidus (D020859)
..expandHemarthrosis (D006395)
..expandHip Dysplasia, Beukes Type (C564185)
..expandHydrarthrosis (D006833)
..expandJoint Deformities, Acquired (D016916)
..expandJoint Instability (D007593) Child17
..expandJoint Loose Bodies (D007594)
..expandLaplane Fontaine Lagardere syndrome (C537869)
..expandLaryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy (C566379)
..expandLeri pleonosteosis (C537118)
..expandMetatarsalgia (D037061)
..expandMorillo-Cucci Passarge syndrome (C536983)
..expandNail-Patella Syndrome (D009261) Child1
..expandOsteoarthropathy, Primary Hypertrophic (D010004) Child2
..expandOsteoarthropathy, Secondary Hypertrophic (D010005)
..expandPatellofemoral Pain Syndrome (D046788)
..expandPfeiffer Palm Teller syndrome (C537889)
..expandShort stature and locking fingers (C537603)
..expandShoulder Impingement Syndrome (D019534)
..expandSynovitis (D013585) Child5
..expandTemporomandibular Joint Disorders (D013705) Child2
..expandThai Symphalangism Syndrome (C564303)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:718
Name:Ankylosis
Definition:Fixation and immobility of a joint.
Alternative IDs:
ParentIDs:MESH:D007592
TreeNumbers:C05.550.069
Synonyms:Ankyloses
Slim Mappings:Musculoskeletal disease
Reference: MedGen: D000844
MeSH: D000844
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants