Metadata | |
---|---|
ID | DOID:2736 |
Name | Hajdu-Cheney syndrome |
Definition | A bone disease characterized by short stature, coarse and dysmorphic facies, bowing of the long bones, and vertebral anomalies that has_material_basis_in heterozygous mutation in the NOTCH2 gene on chromosome 1p12. https://www.ncbi.nlm.nih.gov/pubmed/21378985, https://www.ncbi.nlm.nih.gov/pubmed/21378989, https://www.ncbi.nlm.nih.gov/pubmed/9714016 |
Xrefs |
SNOMEDCT_US_2023_03_01:63122002 |
Alternateids |
DOID:2735 |
Subsets |
DO_rare_slim NCIthesaurus |
Synonyms |
acroosteolysis with osteoporosis and changes in skull and mandible [EXACT] arthrodentoosteodysplasia [EXACT] Cheney syndrome [EXACT] HJCYS [EXACT] serpentine fibula-polycystic kidney syndrome [EXACT] SFPKS [EXACT] |
Parent Relationships |
is_a bone disease |