| Disease Browser
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Parent Node:
 Joint Diseases (D007592) |
Parent Node:
Muscular Diseases (D009135) |
Parent Node:
Musculoskeletal Abnormalities (D009139) |
..Starting node
.. Arthrogryposis (D001176)
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Child Nodes:
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| ........Arthrogryposis and ectodermal dysplasia (C537441) |
| ........Arthrogryposis epileptic seizures migrational brain disorder (C537442) |
| ........Arthrogryposis multiplex congenita neurogenic type (C536614) |
| ........Arthrogryposis multiplex congenita whistling face (C538401) |
| ........Arthrogryposis multiplex congenita, distal type 1 (C535378) |
| ........Arthrogryposis multiplex congenita, distal type 2 (C535379) |
| ........Arthrogryposis multiplex congenita, distal, X-linked (C535380) |
| ........Arthrogryposis multiplex with deafness, inguinal hernias, and early death (C535381) |
| ........Arthrogryposis renal dysfunction cholestasis syndrome (C535382) |
| ........ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED (OMIM:300158) |
| ........Arthrogryposis, Distal, Type 10 (C566069) |
| ........ARTHROGRYPOSIS, DISTAL, TYPE 1A (OMIM:108120) |
| ........Arthrogryposis, distal, type 2E (C535384) |
| ........Arthrogryposis, Distal, Type 4 (C563791) |
| ........Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies (C535385) |
| ........Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies (C565940) |
| ........Arthrogryposis, X-Linked, Type V (C564574) |
| ........Arthrogryposis-like hand anomaly and sensorineural deafness (C535386) |
| ........Boylan Dew Greco syndrome (C537083) |
| ........Bruck syndrome 1 (C537406) |
| ........Bruck syndrome 2 (C537407) |
| ........Camptodactyly-ichthyosis syndrome (C537976) |
| ........Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome (C566861) |
| ........Cerebrooculofacioskeletal Syndrome 2 (C565185) |
| ........Cerebrooculofacioskeletal Syndrome 4 (C565184) |
| ........Contractures ectodermal dysplasia cleft lip palate (C535465) |
| ........Cyprus facial neuromusculoskeletal syndrome (C536229) |
| ........Distal arthrogryposis Moore Weaver type (C536814) |
| ........Distal arthrogryposis type 2B (C538400) |
| ........EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776) |
| ........German Syndrome (C562543) |
| ........Gordon syndrome (C537288) |
| ........Hecht syndrome (C535857) |
| ........Holoprosencephaly with Fetal Akinesia/Hypokinesia Sequence (C564409) |
| ........Jequier Kozlowski skeletal dysplasia (C537569) |
| ........Johnston Aarons Schelley syndrome (C535883) |
| ........Kuskokwim disease (C538124) |
| ........Ladda Zonana Ramer syndrome (C538135) |
| ........Lethal Arthrogryposis With Anterior Horn Cell Disease (C567502) |
| ........Lethal congenital contracture syndrome 1 (C537194) |
| ........Lethal Congenital Contracture Syndrome 2 (C564369) |
| ........Massa Casaer Ceulemans syndrome (C536031) |
| ........Minicore myopathy, antenatal onset, with arthrogryposis (C537474) |
| ........Multiple Pterygium Syndrome, Autosomal Dominant (C566739) |
| ........MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE (OMIM:253290) |
| ........Muscular Dystrophy, Congenital, Producing Arthrogryposis (C564985) |
| ........Neuropathy, congenital, with arthrogryposis multiplex (C535714) |
| ........Oculomelic amyoplasia (C537737) |
| ........Pelvic dysplasia arthrogryposis of lower limbs (C535548) |
| ........Pena Shokeir syndrome, type 1 (C536647) |
| ........Podder-Tolmie syndrome (C537518) |
| ........Ray Peterson Scott syndrome (C535292) |
| ........Spondylohypoplasia, arthrogryposis and popliteal pterygium (C535790) |
| ........Spranger Schinzel Myers syndrome (C535801) |
| ........Tomaculous neuropathy (C536965) |
Sister Nodes: |
..Absent patella (C535568)
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..ACROPECTOROVERTEBRAL DYSPLASIA (OMIM:102510)
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..Arthrogryposis (D001176)  55
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..Campomelic Dysplasia (D055036) 6
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..Cervical Rib Syndrome (D002573) 1
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..Chondrodysplasia, Grebe type (C537915)
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..Congenital absence of gluteal muscles (C535561)
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..Congenital absence of the sternocleidomastoid muscle (C535977)
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..Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi (C567863)
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..Craniofacial Abnormalities (D019465) 685
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..Funnel Chest (D005660) 4
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..Gastroschisis (D020139) 1
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..Hajdu-Cheney Syndrome (D031845) 1
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..Hip Dislocation, Congenital (D006618) 12
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..Klippel-Feil Syndrome (D007714) 5
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..Larsen syndrome, recessive type (C537874)
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..Laryngomalacia (D055092) 1
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..Limb Deformities, Congenital (D017880) 495
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..Pectus Carinatum (D066166)
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..Pseudoarthrogryposis (C566753)
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..Pterygium, Antecubital (C566738)
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..Sacrococcygeal dysgenesis association (C537225)
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..Sternal cleft (C537489)
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..Synostosis (D013580) 150
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..Tracheobronchomalacia (D055089) 4
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..VACTERL Association With Hydrocephalus (C564751)
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..Widow's Peak Syndrome (C564040)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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