Two syndromes of oral, facial, and digital malformations. Type I (Papillon-Leage and Psaume syndrome, Gorlin-Psaume syndrome) is inherited as an X-linked dominant trait and is found only in females and XXY males. Type II (Mohr syndrome) is inherited as an autosomal recessive trait.

Descriptor ID	D009958
MeSH Number(s)	C05.116.099.370.652 C05.660.207.700 C16.131.077.677 C16.131.260.830.670 C16.131.621.207.700 C16.320.180.830.670
Concept/Terms	Orofaciodigital Syndromes Orofaciodigital Syndromes Syndrome, Orofaciodigital Syndromes, Orofaciodigital Oral-Facial-Digital Syndrome Orofaciodigital Syndrome Orodigitofacial Dysostosis Orodigitofacial Syndrome Dysplasia Linguofacialis Oro-Facio-Digital Syndrome Papillon-Leage and Psaume Syndrome Papillon-Leage and Psaume Syndrome Papillon Leage and Psaume Syndrome Oral-Facial-Digital Syndrome, Type I Oral Facial Digital Syndrome, Type I Orofaciodigital Syndrome I Orofaciodigital Syndrome Is Gorlin-Psaume Syndrome Gorlin Psaume Syndrome Syndrome, Gorlin-Psaume Mohr Syndrome Mohr Syndrome Syndrome, Mohr Orofaciodigital Syndrome II Orofaciodigital Syndrome IIs Oral-Facial-Digital Syndrome, Type II Oral Facial Digital Syndrome, Type II

Below are MeSH descriptors whose meaning is more general than "Orofaciodigital Syndromes".

Below are MeSH descriptors whose meaning is related to "Orofaciodigital Syndromes".

Below are MeSH descriptors whose meaning is more specific than "Orofaciodigital Syndromes".