Human genes for acromelic frontonasal dysostosis
Acromelic frontonasal dysostosis [DOID:0060342]
A dysostosis characterized by cranium bifidum, severe hypertelorism, median cleft lip and palate, nasal bifurcation, brachycephaly, large fontanelle, tibial hemimelia, preaxial polydactyly of the feet and brain malformations.
Synonyms: acromelic frontonasal dysostosis, acromelic frontonasal dysostosises, DOID:0060342