(Q27677638)
English
Axenfeld-Rieger syndrome type 1
Axenfeld-Rieger syndrome that has material basis in heterozygous mutation in the homeobox transcription factor gene PITX2 on chromosome 4q25
- RIEG1
- Rieger syndrome type 1
- Rieg
- Rieger Syndrome, Type 1
- Rgs
- AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1
- AXENFELD-RIEGER SYNDROME, TYPE 1
Statements
1 reference
C75015
1 reference
Identifiers
1 reference
2 references
1 reference
1 reference
1 reference