| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Craniofacial Abnormalities (D019465) |
Parent Node:
Growth Disorders (D006130) |
Parent Node:
Hand Deformities, Congenital (D006228) |
Parent Node:
Intellectual Disability (D008607) |
Parent Node:
Joint Diseases (D007592) |
..Starting node
.. Morillo-Cucci Passarge syndrome (C536983)
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Child Nodes:
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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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..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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..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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..Growth mental deficiency syndrome of Myhre (C537620)
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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 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, CTD
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