Term ID: | 6197 |
Name: | Laplane Fontaine Lagardere syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D004392|MESH:D007592|MESH:D010009|MESH:D013122 |
TreeNumbers: | C05.116.099.343/C537869 |C05.116.099.708/C537869 |C05.116.900/C537869 |C05.550/C537869 |C16.320.240/C537869 |C19.297/C537869 |
Synonyms: | Familial syndesmodysplasic dwarfism |Syndesmodysplasic Dwarfism |
Slim Mappings: | Endocrine system disease|Genetic disease (inborn)|Musculoskeletal disease |
Reference: |
MedGen: C537869
MeSH: C537869
OMIM:
Genes: |
Phenotypes | |
Disease Causing ClinVar Variants | |