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loading...| Preferred Name | Kenny-Caffey Syndrome | |
| Synonyms |
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| 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. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C130991 |
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| 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. |
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| code |
C130991 |
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| Contributing_Source |
NICHD |
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| 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. |
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| in_subset | ||
| label |
Kenny-Caffey Syndrome |
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| Preferred_Name |
Kenny-Caffey Syndrome |
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| prefixIRI |
NCIT:C130991 |
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| prefLabel |
Kenny-Caffey Syndrome |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0265291 |
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| subClassOf |
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