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arthrogryposis
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Summary
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
ERGIC1
LGI4
MYH3
TNNT3
AMCN
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
contractile fiber
muscle contraction
EBAUER_MYOGENIC_TARGETS_OF_PAX3_FOXO1_FUSION
MODULE_201
DELASERNA_TARGETS_OF_MYOD_AND_SMARCA4
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Curated Studies
Most Correlated Studies
OMIM - Alkuraya-Kucinskas syndrome
OMIM - Van den Ende-Gupta syndrome
OMIM - Wieacker-Wolff syndrome
OMIM - Disorder of brain
OMIM - Arthrogryposis
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Literature
Most Relevant Literature
Ichthyosis, petechiae, and arthrogryposis in a neonate.
Neurogenic arthrogryposis and the power of phenotyping.
Neonatal developmental and epileptic encephalopathy with movement disorders and arthrogryposis: A ca…
PIEZO2-related distal arthrogryposis type 5: Longitudinal follow-up of a three-generation family bro…
Bi-allelic loss of ERGIC1 causes relatively mild arthrogryposis.
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Clinical Trials
Most Relevant Clinical Trials
Pediatric and Adult Registry for Patients With ARThrogryposis
Arthrogryposis Multiplex Congenita in Pediatric Age: Correlation Between MUScular MRI and Functional…
Mercuri Analysis Contribution on Handicap Evaluation in ArthrogypOsis, a Congenital Neuromuscular Di…
Study of Resting and Exercising Body Functioning in Freeman-Sheldon Syndrome and Related Conditions
Survey Study and Records Review of Treatment Outcomes in Freeman-Sheldon Syndrome
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