loading...| Preferred Name |
Rieger Syndrome |
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| Synonyms |
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| Definitions |
A congenital condition associated with mutation(s) in the PITX2 and/or FOXC1 genes, encoding pituitary homeobox 2 and forkhead box protein C1, respectively. The condition is characterized by anterior segment dysgenesis of the eye(s), iris and corneal anomalies, glaucoma, craniofacial anomalies, hypodontia, and pituitary hypoplasia with hypopituitarism, and hypospadius. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C131001 |
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| ALT_DEFINITION |
A congenital condition associated with mutation(s) in the PITX2 and/or FOXC1 genes, encoding pituitary homeobox 2 and forkhead box protein C1, respectively. The condition is characterized by anterior segment dysgenesis of the eye(s), iris and corneal anomalies, glaucoma, craniofacial anomalies, hypodontia, and pituitary hypoplasia with hypopituitarism, and hypospadius. |
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| code |
C131001 |
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| Contributing_Source |
Cellosaurus NICHD |
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| definition |
A congenital condition associated with mutation(s) in the PITX2 and/or FOXC1 genes, encoding pituitary homeobox 2 and forkhead box protein C1, respectively. The condition is characterized by anterior segment dysgenesis of the eye(s), iris and corneal anomalies, glaucoma, craniofacial anomalies, hypodontia, and pituitary hypoplasia with hypopituitarism, and hypospadius. |
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| in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 |
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| label |
Rieger Syndrome |
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| Preferred_Name |
Rieger Syndrome |
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| prefixIRI |
NCIT:C131001 |
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| prefLabel |
Rieger Syndrome |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C3495488 |
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| subClassOf |