Preferred Label : Acrofacial dysostosis, Palagonia type;
ICD-11 definition : Acrofacial dysostosis, palagonia type belong to the group of acrofacial dysostoses,
and is a very rare condition of mild severity characterized by shortness of stature,
normal IQ and mild acrofacial dysostosis (malar hypoplasia, micrognathia and webbing
of digits with shortening of the fourth metacarpals) associated with oligodontia or
supernumerary teeth, mild vertebral anomalies, scalp or hair defects (aplasia cutis
congenita and pili torti), and cleft lip.;
Origin ID : 656294814;
Automatic exact mappings (from CISMeF team)
Acrofacial dysostosis, palagonia type belong to the group of acrofacial dysostoses,
and is a very rare condition of mild severity characterized by shortness of stature,
normal IQ and mild acrofacial dysostosis (malar hypoplasia, micrognathia and webbing
of digits with shortening of the fourth metacarpals) associated with oligodontia or
supernumerary teeth, mild vertebral anomalies, scalp or hair defects (aplasia cutis
congenita and pili torti), and cleft lip.