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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 cataracts, poor growth, and dysmorphic facies
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Accession:DOID:0070346 term browser browse the term
Definition:A syndrome that is characterized by impaired intellectual development with absent language and short stature and that has_material_basis_in homozygous mutation in the INTS1 gene on chromosome 7p22. (DO)
Synonyms:exact_synonym: NDCAGF
 primary_id: MIM:618571
 xref: EFO:0010561


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neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G INTS1 integrator complex subunit 1 ISO ClinVar Annotator: match by term: Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies OMIM
ClinVar		 PMID:16199547 PMID:25741868 PMID:28492532 PMID:28542170 PMID:28763441 More... NCBI chr 6:15,453,491...15,483,240
Ensembl chr 6:15,447,391...15,483,239 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15728
    syndrome 10503
      neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies 1
Path 2
Term Annotations click to browse term
  disease 15728
    disease of anatomical entity 15372
      nervous system disease 13495
        Neurologic Manifestations 9974
          sensory system disease 6995
            eye disease 3581
              lens disease 521
                cataract 511
                  neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies 1
paths to the root