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ONTOLOGY REPORT - ANNOTATIONS


Term:Polycystic Kidneys, Severe Infantile with Tuberous Sclerosis
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Accession:DOID:9004415 term browser browse the term
Synonyms:exact_synonym: CHROMOSOME 16p13.3 DELETION SYNDROME, DISTAL;   PKDTS;   Polycystic Kidney Disease, Infantile Severe, With Tuberous Sclerosis;   Tuberous sclerosis-polycystic kidney disease contiguous gene syndrome
 primary_id: MESH:C536328;   RDO:0001868
 alt_id: OMIM:600273
For additional species annotation, visit the Alliance of Genome Resources.


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Path 1
Term Annotations click to browse term
  disease 16021
    disease of cellular proliferation 5889
      Hamartoma 136
        tuberous sclerosis 101
          Polycystic Kidneys, Severe Infantile with Tuberous Sclerosis 0
Path 2
Term Annotations click to browse term
  disease 16021
    Developmental Diseases 9337
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8165
        genetic disease 7689
          monogenic disease 5447
            autosomal genetic disease 4411
              autosomal dominant disease 2754
                complex cortical dysplasia with other brain malformations 528
                  Malformations of Cortical Development, Group I 378
                    tuberous sclerosis 101
                      Polycystic Kidneys, Severe Infantile with Tuberous Sclerosis 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.