Term ID: | 6792 |
Name: | Marfanoid Mental Retardation Syndrome, Autosomal |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D008382|MESH:D008607|MESH:D019066 |
TreeNumbers: | C05.116.099.674/C565410 |C10.597.606.643/C565410 |C14.240.400.725/C565410 |C14.280.400.725/C565410 |C16.131.077.550/C565410 |C16.131.240.400.720/C565410 |C16.320.540/C565410 |C17.300.500/C565410 |C23.550.291.812/C565410 |C23.888.592.604.646/C565410 |F03.550.600/C5 |
Synonyms: | |
Slim Mappings: | Cardiovascular disease|Congenital abnormality|Connective tissue disease|Genetic disease (inborn)|Mental disorder|Musculoskeletal disease|Nervous system disease|Pathology (process)|Signs and symptoms |
Reference: |
MedGen: C565410
MeSH: C565410
OMIM: 248770;
Genes: |
Phenotypes | |
Disease Causing ClinVar Variants | |