Concept information
Preferred term
Axenfeld syndrome
Definition(s)
- Axenfeld syndrome is a rare autosomal dominant disorder, which affects the development of the teeth, eyes, and abdominal region. (Wikipedia)
Broader concept(s)
In other languages
-
French
-
embryotoxon postérieur
URI
http://data.loterre.fr/ark:/67375/VH8-SKWSL2D0-1
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