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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination
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Accession:DOID:9000512 term browser browse the term
Definition:NEDMEHM is caused by compound heterozygous mutation in the MTHFS gene on chromosome 15q25. (OMIM)
Synonyms:exact_synonym: MTHFS-RELATED CONDITION;   NEDMEHM
 primary_id: OMIM:618367
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13654
    Developmental Disease 10118
      Neurodevelopmental Disorders 5541
        Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination 0
Path 2
Term Annotations click to browse term
  disease 13654
    Developmental Disease 10118
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8607
        genetic disease 8169
          monogenic disease 6395
            autosomal genetic disease 5588
              autosomal dominant disease 3964
                complex cortical dysplasia with other brain malformations 1155
                  Malformations of Cortical Development, Group I 1020
                    microcephaly 866
                      Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination 0
paths to the root