(Q27164456)
English
Axenfeld-Rieger syndrome type 3
Axenfeld-Rieger syndrome that has material basis in heterozygous mutation in the FOXC1 gene on chromosome 6p25
- Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss
- RIEG3
- Rieger syndrome type 3
- anterior chamber cleavage syndrome
- anterior segment mesenchymal dysgenesis
- Axenfeld Anomaly
- AXENFELD-RIEGER SYNDROME, TYPE 3
- Rieger Syndrome, Type 3
- Axenfeld-Rieger Anomaly
- Rieger Anomaly
- AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3
Statements
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743.44
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Identifiers
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