ONTOLOGY REPORT - ANNOTATIONS


Term:Atkin Syndrome
go back to main search page
Accession:DOID:9004603 term browser browse the term
Synonyms:exact_synonym: Atkin Flaitz Patil Smith syndrome;   Atkin-Flaitz syndrome;   X-linked mental retardation syndrome, Atkin type;   X-linked mental retardation, Atkin type;   X-linked mental retardation, nonspecific;   X-linked mental retardation, nonspecific, type 1
 primary_id: MESH:C538195
 alt_id: OMIM:300431;   RDO:0004138
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
Atkin Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Iqsec2 IQ motif and Sec7 domain 2 JBrowse link X 22,212,137 22,293,810 RGD:8554872
G Smc1a structural maintenance of chromosomes 1A JBrowse link X 21,710,976 21,755,708 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14823
    syndrome 4218
      Atkin Syndrome 2
Path 2
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        central nervous system disease 6908
          brain disease 6412
            disease of mental health 4323
              developmental disorder of mental health 2594
                specific developmental disorder 1329
                  intellectual disability 1157
                    syndromic intellectual disability 211
                      Mental Retardation, X-Linked 198
                        Atkin Syndrome 2
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.