loading...| Preferred Name |
Kenny-Caffey Syndrome |
|
| Synonyms |
Kenny-Caffey Syndrome |
|
| Definitions |
A genetic condition characterized by long bone sclerosis and thickening, short stature, and head and eye anomalies. Many affected individuals have hypoparathyroidism with hypocalcemia. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C130991 |
|
| ALT_DEFINITION |
A genetic condition characterized by long bone sclerosis and thickening, short stature, and head and eye anomalies. Many affected individuals have hypoparathyroidism with hypocalcemia. |
|
| code |
C130991 |
|
| Concept_In_Subset | ||
| Contributing_Source |
NICHD |
|
| DEFINITION |
A genetic condition characterized by long bone sclerosis and thickening, short stature, and head and eye anomalies. Many affected individuals have hypoparathyroidism with hypocalcemia. |
|
| FULL_SYN |
Kenny-Caffey Syndrome |
|
| label |
Kenny-Caffey Syndrome |
|
| Preferred_Name |
Kenny-Caffey Syndrome |
|
| prefixIRI |
Thesaurus:C130991 |
|
| Semantic_Type |
Disease or Syndrome |
|
| UMLS_CUI |
C0265291 |
|
| subClassOf |