Imported Annotations - ClinVar
autosomal dominant distal hereditary motor neuronopathy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Autosomal dominant distal hereditary motor neuropathy ClinVar PMID:15668982 more ... autosomal dominant distal hereditary motor neuronopathy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Autosomal dominant distal hereditary motor neuropathy ClinVar PMID:10463355 more ... autosomal dominant distal hereditary motor neuronopathy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Autosomal dominant distal hereditary motor neuropathy ClinVar PMID:22526352 autosomal dominant distal hereditary motor neuronopathy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Autosomal dominant distal hereditary motor neuropathy ClinVar PMID:1520078 more ... bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:10463355 more ... bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:20577006 more ... bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:22419508 more ... bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:27530454 bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:11891693 more ... bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:19232556 more ... bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:18587396 more ... bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:12884428 , PMID:20503319 bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:20503319 bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:19232556 bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:20425821 more ... bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:21964829 bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:20425821 bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:20577006 bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:18587396 bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:19232556 , PMID:20425821 bone development disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:21115951 brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:25741868 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:22689196 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:22851605 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:22419508 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:19666518 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:22851605 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:22851605 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyrachia ClinVar PMID:18587396 brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyrachia ClinVar PMID:18587396 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyrachia ClinVar PMID:11891693 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyrachia ClinVar PMID:25741868 brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyrachia ClinVar PMID:25741868 , PMID:26467025 brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyrachia ClinVar PMID:11891693 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyrachia ClinVar PMID:25741868 more ... brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:28492532 brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:25741868 , PMID:28492532 brachyolmia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia ClinVar PMID:26467025 , PMID:28492532 Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia Maroteaux type ClinVar PMID:20425821 more ... Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 2 ClinVar PMID:25741868 , PMID:26467025 Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 2 ClinVar PMID:25741868 more ... Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 2 ClinVar PMID:25741868 , PMID:28492532 Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 2 ClinVar PMID:25741868 Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 2 ClinVar PMID:11891693 more ... Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia Maroteaux type ClinVar PMID:11891693 more ... Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 2 ClinVar PMID:11891693 more ... Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia Maroteaux type ClinVar PMID:20503319 Brachyolmia Type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia Maroteaux type ClinVar PMID:12884428 , PMID:20503319 Brachyolmia Type 3 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 3 ClinVar PMID:25741868 , PMID:26467025 Brachyolmia Type 3 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 3 ClinVar PMID:25741868 more ... Brachyolmia Type 3 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 3 ClinVar PMID:25741868 Brachyolmia Type 3 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 3 ClinVar PMID:25741868 , PMID:28492532 Brachyolmia Type 3 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia Type 3 ClinVar PMID:11891693 more ... Brachyolmia Type 3 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia autosomal dominant ClinVar PMID:11891693 more ... Brachyolmia Type 3 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Brachyolmia autosomal dominant ClinVar PMID:18587396 more ... Brachyolmia Type 3 ISO RGD:1604803 8554872 ClinVar Annotator: match by OMIM:113500 ClinVar PMID:18587396 Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:22419508 more ... Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:22851605 Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:24789864 Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:25802885 Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:28492532 Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:20037587 more ... Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:1520078 more ... Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:15668982 more ... Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:20037586 more ... Charcot-Marie-Tooth disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:11891693 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 2C ClinVar PMID:10463355 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:21964829 , PMID:28492532 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:20037588 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:20577006 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:20577006 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 2C ClinVar PMID:25802885 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:22419508 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:25741868 , PMID:26467025 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:25741868 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:25741868 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:11891693 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:11891693 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:19232556 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:20460441 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:19661060 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:26392352 , PMID:28492532 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2C ClinVar PMID:20037586 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:11891693 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2C ClinVar PMID:1520078 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:15668982 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2C ClinVar PMID:20037586 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2C ClinVar PMID:21115951 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:20037586 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:27066566 , PMID:28492532 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:26467025 , PMID:28492532 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2C ClinVar PMID:20037587 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:26467025 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:22851605 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:22851605 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:19666518 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:18587396 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:22851605 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:11891693 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:28492532 , PMID:31041394 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:25741868 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:25741868 , PMID:28492532 Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease axonal type 2C ClinVar PMID:22689196 more ... Charcot-Marie-Tooth disease axonal type 2C ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy Type 2C ClinVar PMID:28492532 Charcot-Marie-Tooth disease type 1 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type I ClinVar Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2 ClinVar PMID:25741868 , PMID:28492532 Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar PMID:22689196 more ... Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar PMID:22419508 more ... Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar PMID:22851605 more ... Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar PMID:19666518 more ... Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar PMID:22851605 more ... Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar PMID:26467025 , PMID:28492532 Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar PMID:25741868 more ... Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar PMID:28492532 Charcot-Marie-Tooth disease type 2 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth, Type 2 ClinVar PMID:22851605 more ... Charcot-Marie-Tooth disease type 4 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 4 ClinVar Charcot-Marie-Tooth disease type 4 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 4 ClinVar PMID:28492532 clubfoot ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Talipes equinovarus ClinVar PMID:20037587 more ... Digital Arthropathy-Brachydactyly, Familial ISO RGD:1604803 8554872 ClinVar Annotator: match by OMIM:606835 ClinVar Digital Arthropathy-Brachydactyly, Familial ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Digital arthropathy-brachydactyly, familial ClinVar PMID:25741868 , PMID:26467025 Digital Arthropathy-Brachydactyly, Familial ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Digital arthropathy-brachydactyly, familial ClinVar PMID:25741868 more ... Digital Arthropathy-Brachydactyly, Familial ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Digital arthropathy-brachydactyly, familial ClinVar PMID:25741868 , PMID:28492532 Digital Arthropathy-Brachydactyly, Familial ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Digital arthropathy-brachydactyly, familial ClinVar PMID:25741868 Digital Arthropathy-Brachydactyly, Familial ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Digital arthropathy-brachydactyly, familial ClinVar PMID:11891693 more ... Digital Arthropathy-Brachydactyly, Familial ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Digital arthropathy-brachydactyly, familial ClinVar PMID:11891693 more ... Digital Arthropathy-Brachydactyly, Familial ISO RGD:1604803 8554872 ClinVar Annotator: match by OMIM:606835 ClinVar PMID:21964574 Digital Arthropathy-Brachydactyly, Familial ISO RGD:1604803 8554872 ClinVar Annotator: match by OMIM:606835 ClinVar PMID:11891693 , PMID:21964574 distal hereditary motor neuronopathy type 7B ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Genetic motor neuron disease ClinVar PMID:20037586 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:25741868 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:22851605 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:22689196 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:10463355 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII ClinVar PMID:25741868 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII ClinVar PMID:25741868 distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII ClinVar PMID:11891693 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:19666518 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:22851605 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:20037586 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:22419508 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:15668982 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:20037586 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:22851605 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:11891693 more ... distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII ClinVar distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:25741868 , PMID:26467025 distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:28492532 distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:25741868 , PMID:28492532 distal hereditary motor neuronopathy type 8 ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive ClinVar PMID:26467025 , PMID:28492532 Femur Head Necrosis ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Avascular necrosis of femoral head, primary, 2 ClinVar PMID:11891693 more ... Femur Head Necrosis ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Avascular necrosis of femoral head, primary, 2 ClinVar PMID:25741868 , PMID:26467025 Femur Head Necrosis ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Avascular necrosis of femoral head, primary, 2 ClinVar PMID:25741868 more ... Femur Head Necrosis ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Avascular necrosis of femoral head, primary, 2 ClinVar PMID:25741868 , PMID:28492532 Femur Head Necrosis ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Avascular necrosis of femoral head, primary, 2 ClinVar PMID:25741868 Femur Head Necrosis ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Avascular necrosis of femoral head, primary, 2 ClinVar PMID:11891693 more ... genetic disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:11891693 more ... genetic disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:11891693 more ... genetic disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:11891693 more ... genetic disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:11891693 more ... genetic disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:11891693 more ... Hyponatremia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Sodium serum level quantitative trait locus 1 ClinVar PMID:25741868 , PMID:26467025 Hyponatremia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Sodium serum level quantitative trait locus 1 ClinVar PMID:25741868 more ... Hyponatremia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Sodium serum level quantitative trait locus 1 ClinVar PMID:25741868 , PMID:28492532 Hyponatremia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Sodium serum level quantitative trait locus 1 ClinVar PMID:25741868 Hyponatremia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Sodium serum level quantitative trait locus 1 ClinVar PMID:11891693 more ... Hyponatremia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Sodium serum level quantitative trait locus 1 ClinVar PMID:19666518 more ... Hyponatremia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Sodium serum level quantitative trait locus 1 ClinVar PMID:11891693 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:22851605 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:22419508 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:25741868 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:25741868 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:11891693 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:22689196 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:27530454 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:11891693 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:19666518 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:22851605 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:22851605 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatropic dwarfism ClinVar PMID:11891693 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:25741868 , PMID:26467025 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:28492532 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:20425821 , PMID:20577006 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:20425821 more ... metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:19232556 , PMID:20425821 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:20425821 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:20577006 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:25741868 , PMID:28492532 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:21964829 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:26467025 , PMID:28492532 metatropic dysplasia ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Metatrophic dysplasia ClinVar PMID:25741868 more ... neuromuscular disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Neuromuscular disease ClinVar PMID:18587396 more ... neuromuscular disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Neuromuscular Diseases ClinVar PMID:20037586 more ... neuromuscular disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Neuromuscular Diseases ClinVar PMID:1520078 more ... neuromuscular disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Neuromuscular Diseases ClinVar PMID:15668982 more ... neuromuscular disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Neuromuscular Diseases ClinVar PMID:20037587 more ... neuromuscular disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Neuromuscular Diseases ClinVar PMID:20037586 more ... neuromuscular disease ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Neuromuscular disease ClinVar PMID:11891693 more ... parastremmatic dwarfism ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Parastremmatic dwarfism ClinVar PMID:25741868 , PMID:26467025 parastremmatic dwarfism ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Parastremmatic dwarfism ClinVar PMID:25741868 more ... parastremmatic dwarfism ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Parastremmatic dwarfism ClinVar PMID:25741868 , PMID:28492532 parastremmatic dwarfism ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Parastremmatic dwarfism ClinVar PMID:25741868 parastremmatic dwarfism ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Parastremmatic dwarfism ClinVar PMID:11891693 more ... parastremmatic dwarfism ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Parastremmatic dwarfism ClinVar PMID:19232556 more ... parastremmatic dwarfism ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Parastremmatic dwarfism ClinVar PMID:11891693 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:25741868 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:22851605 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:22689196 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:22419508 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal Form of Spinal Muscular Atrophy ClinVar PMID:25741868 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal Form of Spinal Muscular Atrophy ClinVar PMID:25741868 scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal Form of Spinal Muscular Atrophy ClinVar PMID:11891693 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:19666518 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:22851605 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:1520078 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:15668982 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:20037586 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:22851605 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Amyotrophy, neurogenic scapuloperoneal, New England type ClinVar PMID:11891693 more ... scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal Spinal Muscular Atrophy ClinVar scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:25741868 , PMID:26467025 scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:28492532 scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:25741868 , PMID:28492532 scapuloperoneal spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Scapuloperoneal spinal muscular atrophy ClinVar PMID:26467025 , PMID:28492532 spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy ClinVar PMID:20037586 more ... spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy ClinVar PMID:25741868 more ... spinal muscular atrophy ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Distal spinal muscular atrophy ClinVar PMID:28492532 spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:25741868 more ... spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:22851605 more ... spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:22689196 more ... spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:22419508 more ... spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:19666518 more ... spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:22851605 more ... spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:22851605 more ... spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:28492532 spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:25741868 , PMID:28492532 spondyloepimetaphyseal dysplasia, Strudwick type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia ClinVar PMID:26467025 , PMID:28492532 spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: PSEUDO-MORQUIO SYNDROME, TYPE 2 ClinVar PMID:25741868 , PMID:26467025 spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: PSEUDO-MORQUIO SYNDROME, TYPE 2 ClinVar PMID:25741868 more ... spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: PSEUDO-MORQUIO SYNDROME, TYPE 2 ClinVar PMID:25741868 , PMID:28492532 spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: PSEUDO-MORQUIO SYNDROME, TYPE 2 ClinVar PMID:25741868 spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: PSEUDO-MORQUIO SYNDROME, TYPE 2 ClinVar PMID:11891693 more ... spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondyloepiphyseal dysplasia Maroteaux type ClinVar PMID:11891693 more ... spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: SED, Maroteaux type ClinVar PMID:11891693 more ... spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by OMIM:184095 ClinVar PMID:12884428 , PMID:20503319 spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by OMIM:184095 ClinVar PMID:20425821 more ... spondyloepiphyseal dysplasia Maroteaux type ISO RGD:1604803 8554872 ClinVar Annotator: match by OMIM:184095 ClinVar PMID:20503319 spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia, Kozlowski type ClinVar PMID:20577006 more ... spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia, Kozlowski type ClinVar PMID:25741868 , PMID:26467025 spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia, Kozlowski type ClinVar PMID:25741868 more ... spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia, Kozlowski type ClinVar PMID:25741868 , PMID:28492532 spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia, Kozlowski type ClinVar PMID:11891693 more ... spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia, Kozlowski type ClinVar PMID:19232556 more ... spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: SMD Kozlowski type ClinVar PMID:11891693 more ... spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by term: Spondylometaphyseal dysplasia, Kozlowski type ClinVar PMID:25741868 spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by OMIM:184252 ClinVar PMID:20425821 more ... spondylometaphyseal dysplasia Kozlowski type ISO RGD:1604803 8554872 ClinVar Annotator: match by OMIM:184252 ClinVar PMID:19232556 
Gene-Chemical Interaction Annotations
