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RGD uses the Human Disease Ontology (DO, 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:MORM Syndrome
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Accession:DOID:9006992 term browser browse the term
Synonyms:exact_synonym: MORMS;   Mental retardation, truncal Obesity, Retinal dystrophy and Micropenis;   Mental retardation, truncal Obesity, Retinal dystrophy and Micropenis syndrome
 primary_id: MESH:C536984
 alt_id: OMIM:610156
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
MORM Syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Inpp5e inositol polyphosphate-5-phosphatase E ISO ClinVar Annotator: match by OMIM:610156
DNA:nonsense mutation:exon:p.Q627X (c.1879C>T) (human)
ClinVar Annotator: match by term: MORM syndrome
PMID:19668215 PMID:25741868 PMID:28492532 PMID:19668215 RGD:12911209 NCBI chr 3:9,216,776...9,229,539
Ensembl chr 3:9,216,776...9,229,450
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17435
    syndrome 8262
      MORM Syndrome 1
Path 2
Term Annotations click to browse term
  disease 17435
    disease of anatomical entity 16766
      nervous system disease 12209
        central nervous system disease 10477
          brain disease 9840
            disease of mental health 7119
              developmental disorder of mental health 4434
                specific developmental disorder 3680
                  intellectual disability 3492
                    MORM Syndrome 1
paths to the root