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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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Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mthfs 5, 10-methenyltetrahydrofolate synthetase ISO ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND HYPOMYELINATION OMIM
ClinVar
PMID:25741868 PMID:30031689 NCBI chr 9:89,211,190...89,240,225
Ensembl chr 9:89,210,676...89,377,713
JBrowse link
G Mthfsl 5, 10-methenyltetrahydrofolate synthetase-like ISO ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND HYPOMYELINATION ClinVar PMID:25741868 PMID:30031689 NCBI chr 9:88,685,630...88,720,320
Ensembl chr 9:88,688,602...88,720,296
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14274
    Developmental Disease 10452
      Neurodevelopmental Disorders 5650
        Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination 2
Path 2
Term Annotations click to browse term
  disease 14274
    Developmental Disease 10452
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8736
        genetic disease 8279
          monogenic disease 6334
            autosomal genetic disease 5493
              autosomal dominant disease 3754
                complex cortical dysplasia with other brain malformations 1170
                  Malformations of Cortical Development, Group I 1033
                    microcephaly 879
                      Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination 2
paths to the root