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Human Disease and Mouse Model Detail
Human Disease Arthrogryposis, Distal, Type 2B; DA2B
OMIM ID: 601680
Human Phenotype Ontology associations
Synonyms Arthrogryposis Multiplex Congenita, Distal, Type 2B; Arthrogryposis Multiplex Congenita, Distal, Type II, with Craniofacial Abnormalities; Arthrogryposis, Distal; Freeman-Sheldon Syndrome Variant; FSSV; Sheldon-Hall Syndrome; SHS
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     MYH3* Myh3   HomoloGene and HGNC
TNNI2* Tnni2   HomoloGene and HGNC
TNNT3* Tnnt3   HomoloGene and HGNC
TPM2* Tpm2   HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory