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ONTOLOGY REPORT - ANNOTATIONS


Term:agenesis of the corpus callosum with peripheral neuropathy
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Accession:DOID:0090003 term browser browse the term
Definition:A neurodegenerative disease characterized by autosomal recessive inheritance with early onset of severe sensory-motor polyneuropathy, variable degree of agenesis of the corpus callosum, amyotrophy, hypotonia, and cognitive impairment that has_material_basis_in homozygous or compound heterozygous mutation in the SLC12A6 gene on chromosome 15q14. (DO)
Synonyms:exact_synonym: ACCPN;   Agenesis of Corpus Callosum with Peripheral Neuropathy;   Agenesis of Corpus Callosum with Polyneuropathy;   Andermann syndrome;   Charlevoix disease;   Corpus Callosum Agenesis Neuronopathy;   Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum;   agenesis of corpus callosum with neuronopathy;   corpus callosum agenesis-neuronopathy syndrome;   hereditary motor and sensory neuropathy with agenesis of corpus callosum;   polyneuropathy, sensorimotor, with or without agenesis of the corpus callosum
 primary_id: MESH:C536446
 alt_id: DOID:0060600;   OMIM:218000;   RDO:0002040;   RDO:9002736
 xref: ORDO:1496
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agenesis of the corpus callosum with peripheral neuropathy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Emc4 ER membrane protein complex subunit 4 JBrowse link 3 103,852,139 103,857,172 RGD:8554872
G Nop10 NOP10 ribonucleoprotein JBrowse link 3 103,747,654 103,748,739 RGD:8554872
G Slc12a6 solute carrier family 12, member 6 JBrowse link 3 103,752,213 103,852,686 RGD:1580594
RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16017
    disease of anatomical entity 15273
      nervous system disease 10762
        peripheral nervous system disease 2363
          agenesis of the corpus callosum with peripheral neuropathy 3
Path 2
Term Annotations click to browse term
  disease 16017
    Developmental Diseases 9307
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8132
        genetic disease 7652
          monogenic disease 5403
            autosomal genetic disease 4361
              autosomal recessive disease 2342
                agenesis of the corpus callosum with peripheral neuropathy 3
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.