| Disease Browser
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Parent Node:
 Joint Diseases (D007592) |
..Starting node
.. Joint Instability (D007593)
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Child Nodes:
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| ........Achard syndrome (C536012) |
| ........Arterial Tortuosity Syndrome (C565942) |
| ........Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234) |
| ........Brittle cornea syndrome 1 (C536192) |
| ........BRITTLE CORNEA SYNDROME 2 (OMIM:614170) |
| ........CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE (OMIM:614078) |
| ........Daish Hardman Lamont syndrome (C535770) |
| ........Desbuquois syndrome (C535943) |
| ........Dislocation of Hip, Congenital, with Hyperextensibility of Fingers and Facial Dysmorphism (C563315) |
| ........Hemangiomatosis, Cutaneous, with Associated Features (C562438) |
| ........Hypospadias-Mental Retardation Syndrome (C563067) |
| ........Jaffer Beighton syndrome (C537561) |
| ........Joint laxity, familial (C535884) |
| ........Megarbane syndrome (C536145) |
| ........Mental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities (C567209) |
| ........Panic Disorder with Joint Laxity (C566835) |
| ........Patella, Familial Recurrent Dislocation Of (C566816) |
| ........Spondyloepimetaphyseal Dysplasia With Joint Laxity (C562968) |
| ........Spondyloepiphyseal Dysplasia with Atlantoaxial Instability (C563472) |
| ........Van Maldergem Wetzburger Verloes syndrome (C536530) |
| ........Young Simpson syndrome (C536717) |
Sister Nodes: |
..Ankylosis (D000844)  10
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..Arthralgia (D018771) 1
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..Arthritis (D001168) 57
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..Arthrogryposis (D001176) 55
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..Arthropathy, Neurogenic (D001177) 3
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..Arthropathy, progressive pseudorheumatoid, of childhood (C535387)
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..Borrone Di Rocco Crovato syndrome (C536577)
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..Brachydactylous dwarfism Mseleni type (C537086)
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..Bursitis (D002062) 1
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..Calcification of Joints and Arteries (C565891)
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..Chondromatosis, Synovial (D015838) 1
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..Contracture (D003286) 41
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..Coracoclavicular Joint, Anomalous (C565161)
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..Crystal Arthropathies (D000070657)
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..Cushing's symphalangism (C536223)
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..Dwarfism stiff joint ocular abnormalities (C535724)
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..Femoracetabular Impingement (D057925)
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..Flynn Aird syndrome (C537066)
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..GEMSS syndrome (C537679)
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..Hallux Limitus (D020857)
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..Hallux Rigidus (D020859)
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..Hemarthrosis (D006395)
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..Hip Dysplasia, Beukes Type (C564185)
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..Hydrarthrosis (D006833)
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..Joint Deformities, Acquired (D016916)
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..Joint Dislocations (D004204) 16
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..Joint Instability (D007593) 17
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..Joint Loose Bodies (D007594)
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..Laplane Fontaine Lagardere syndrome (C537869)
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..Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy (C566379)
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..Leri pleonosteosis (C537118)
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..Metatarsalgia (D037061)
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..Morillo-Cucci Passarge syndrome (C536983)
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..Nail-Patella Syndrome (D009261) 1
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..Osteoarthropathy, Primary Hypertrophic (D010004) 2
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..Osteoarthropathy, Secondary Hypertrophic (D010005)
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..Patellofemoral Pain Syndrome (D046788)
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..Pfeiffer Palm Teller syndrome (C537889)
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..Short stature and locking fingers (C537603)
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..Shoulder Impingement Syndrome (D019534)
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..Synovitis (D013585) 5
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..Temporomandibular Joint Disorders (D013705) 2
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..Thai Symphalangism Syndrome (C564303)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
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