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loading...| Preferred Name |
Frasier Syndrome |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C122805 |
| ALT_DEFINITION |
A condition, which typically presents during adolescence, that is caused by WT-1 mutation, and is characterized by a developmental sex disorder, FSGS, and may be associated with gonadoblastoma. |
| code |
C122805 |
| Concept_In_Subset | |
| Contributing_Source |
NICHD |
| DEFINITION |
A condition, which typically presents during adolescence, that is caused by WT-1 mutation, and is characterized by a developmental sex disorder, FSGS, and may be associated with gonadoblastoma. |
| Has_NICHD_Parent | |
| label |
Frasier Syndrome |
| NICHD_Hierarchy_Term |
Frasier Syndrome |
| Preferred_Name |
Frasier Syndrome |
| prefixIRI |
C122805 |
| prefLabel |
Frasier Syndrome |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0950122 |
| subClassOf |