Axenfeld-Rieger syndrome type 3
Axenfeld-Rieger syndrome that has material basis in heterozygous mutation in the FOXC1 gene on chromosome 6p25
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Summary
Axenfeld-Rieger syndrome type 3 is a rare disease[1].
Key Facts
- Axenfeld-Rieger syndrome type 3's instance of is recorded as rare disease[2].
- Axenfeld-Rieger syndrome type 3's instance of is recorded as class of disease[3].
- Axenfeld-Rieger syndrome type 3's subclass of is recorded as Axenfeld-Rieger syndrome[4].
- Axenfeld-Rieger syndrome type 3's OMIM ID is recorded as 602482[5].
- Axenfeld-Rieger syndrome type 3's Disease Ontology ID is recorded as DOID:0110122[6].
- Axenfeld-Rieger syndrome type 3's ICD-9-CM is recorded as 743.44[7].
- Axenfeld-Rieger syndrome type 3's health specialty is recorded as medical genetics[8].
- Axenfeld-Rieger syndrome type 3's genetic association is recorded as FOXC1[9].
- Axenfeld-Rieger syndrome type 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110122[10].
- Axenfeld-Rieger syndrome type 3's exact match is recorded as http://identifiers.org/doid/DOID:0110122[11].
- Axenfeld-Rieger syndrome type 3's UMLS CUI is recorded as C0266548[12].
- Axenfeld-Rieger syndrome type 3's UMLS CUI is recorded as C0265341[13].
- Axenfeld-Rieger syndrome type 3's UMLS CUI is recorded as C2678503[14].
- Axenfeld-Rieger syndrome type 3's ICD-10-CM is recorded as triskaidekaphobia.8[15].
- Axenfeld-Rieger syndrome type 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- Axenfeld-Rieger syndrome type 3's Mondo ID is recorded as MONDO_0011233[17].
- Axenfeld-Rieger syndrome type 3's UniProt disease ID is recorded as DI-01266[18].