Term ID: | 4116 |
Name: | Fallot complex with severe mental and growth retardation |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D006130|MESH:D008607|MESH:D013771 |
TreeNumbers: | C10.597.606.643/C536608 |C14.240.400.849/C536608 |C14.280.400.849/C536608 |C16.131.240.400.849/C536608 |C23.550.393/C536608 |C23.888.592.604.646/C536608 |F03.550.600/C536608 |
Synonyms: | Bindewald Ulmer Muller syndrome |
Slim Mappings: | Cardiovascular disease|Congenital abnormality|Mental disorder|Nervous system disease|Pathology (process)|Signs and symptoms |
Reference: |
MedGen: C536608
MeSH: C536608
OMIM: 601127;
Genes: |
Phenotypes | |
Disease Causing ClinVar Variants | |