Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expand
Joint Diseases (D007592)
..Starting node
..expand
Arthritis (D001168)

       Child Nodes:
........expandArthritis, Experimental (D001169)
........expandArthritis, Infectious (D001170) Child2
........expandArthritis, Juvenile (D001171) Child3
........expandArthritis, Psoriatic (D015535)
........expandArthritis, Rheumatoid (D001172) Child9
........expandArthritis, Sacroiliac (C563037)
........expandChondrocalcinosis (D002805) Child3
........expandGout (D006073) Child6
........expandHistiocytic Dermatoarthritis (C564183)
........expandLeukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema (C563852)
........expandLeukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia (C535888)
........expandMeyenburg-Altherr-Uehlinger syndrome (C537574)
........expandNegative rheumatoid factor polyarthritis (C538347)
........expandOsteoarthritis (D010003) Child8
........expandPeriarthritis (D010489)
........expandRheumatic Fever (D012213) Child3
........expandSacroiliitis (D058566)
........expandSpondylarthritis (D025241) Child7
........expandStickler syndrome, type 1 (C537492)
........expandStickler syndrome, type 3 (C537494)



 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:894
Name:Arthritis
Definition:
Alternative IDs:
ParentIDs:MESH:D007592
TreeNumbers:C05.550.114
Synonyms:Arthritides |Polyarthritides |Polyarthritis
Slim Mappings:Musculoskeletal disease
Reference: MedGen: D001168
MeSH: D001168
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants