Kenny-Caffey Syndrome
Disease ID: disease_node_15651
Connections displayed (default: 10).
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| Dbxref | MIM:PS127000, ORDO:2333 |
|---|---|
| Subclassof | DOID_2256, DOID_225 |
| Data Source | DOID |
| Doid Label | Kenny-Caffey syndrome |
| Doid Description | A syndrome that is characterized by growth retardation with proportionate short stature, cortical thickening and medullary stenosis of the long bones, delayed anterior fontanelle closure, hypocalcemia due to congenital hypoparathyroidism and facial dysmorphism, including prominent forehead, microphthalmia, and micrognathia. |
| Has Phenotype | HP_0002652 |
| Disease Node Id | disease_node_15651 |
| Doid Id | DOID_0080724 |
| Label | Kenny-Caffey Syndrome |
- Incoming r'ship
SUBCLASS_OFto/from Kenny-Caffey Syndrome Type 2(ID:disease_node_15652) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Kenny-Caffey Syndrome Type 1(ID:disease_node_15653) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease)