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LD25.00 Oral-facial-digital syndrome

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

A condition caused by failure of the head and digits to correctly develop during the antenatal period. This condition may be associated with cleft or lobed tongue, noncancerous tumours or nodules of the tongue, abnormal shape or number of teeth, cleft palate, hyperplastic frenula of the lip or gums, cleft lip, hypertelorism, wide nose with broad, flat nasal bridge, syndactyly, brachydactyly, clinodactyly, polydactyly, polycystic kidney disease, neurological problems, bone abnormalities, vision loss, or heart defects.

synonyms

• Oral-facial-digital syndrome
• Oral-facial-digital syndrome type 1
• OFD1 - [orolfacialdigital syndrome 1]
• Orofaciodigital syndrome type 1
• Papillon-Léage-Psaume syndrome
• Oral-facial-digital syndrome type 2
• Oral-facial-digital syndrome type 3
• Oral-facial-digital syndrome type 4
• Oral-facial-digital syndrome type 5
• Oral-facial-digital syndrome type 6
• Joubert syndrome with orofaciodigital defect
• Oral-facial-digital syndrome type 8
• Oral-facial-digital syndrome type 9
• Oral-facial-digital syndrome type 10
• Oral-facial-digital syndrome type 11
• Oral-facial-digital syndrome type 12
• Oral-facial-digital syndrome type 13

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