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ONTOLOGY REPORT - ANNOTATIONS


Term:Linear Skin Defects with Multiple Congenital Anomalies 2
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Accession:DOID:9003701 term browser browse the term
Synonyms:exact_synonym: APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIAL DYSMORPHISM, AND OTHER CONGENITAL ANOMALIES;   APLCC;   LSDMCA2
 primary_id: OMIM:300887
 alt_id: RDO:9000176;   RDO:9001634
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Linear Skin Defects with Multiple Congenital Anomalies 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cox7b cytochrome c oxidase subunit 7B JBrowse link X 77,065,427 77,071,676 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15639
    syndrome 5218
      ectodermal dysplasia 251
        Linear Skin Defects with Multiple Congenital Anomalies 2 1
Path 2
Term Annotations click to browse term
  disease 15639
    Developmental Diseases 8774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7556
        genetic disease 7052
          monogenic disease 4684
            autosomal genetic disease 3642
              autosomal dominant disease 2153
                complex cortical dysplasia with other brain malformations 484
                  Malformations of Cortical Development, Group I 340
                    microcephaly 212
                      Linear Skin Defects with Multiple Congenital Anomalies 2 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.