Human Disease and Mouse Model Detail
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Human Disease
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Arthrogryposis, Distal, Type 2B; DA2B
OMIM ID: 601680
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Synonyms
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Arthrogryposis Multiplex Congenita, Distal, Type 2B;
Arthrogryposis Multiplex Congenita, Distal, Type II, with Craniofacial Abnormalities;
Freeman-Sheldon Syndrome Variant; FSSV;
Sheldon-Hall Syndrome; SHS
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Myh3
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MYH3*
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1:1 Homology
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Tnni2
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TNNI2*
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1:1 Homology
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Tnnt3
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TNNT3*
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1:1 Homology
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Tpm2
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TPM2*
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1:1 Homology
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Analysis Tools