C129028Level 6
Frontonasal Dysplasia
**Semantic type:** Disease or Syndrome
**Definition:** Frontonasal dysplasia caused by mutations in the ALX3 gene, encoding homeobox protein aristaless-like 3. It is inherited in an autosomal recessive fashion.
**Synonyms:** - FND1 - Frontonasal Dysplasia 1
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