Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A very rare multiple congenital anomaly syndrome characterized by the presence of anophthalmia or severe microphthalmia, cleft lip/palate, facial cleft and sacral neural tube defects, along with various additional anomalies including congenital glaucoma, iris coloboma, primary hyperplastic vitreous, hypertelorism, low-set ears, clinodactyly, choanal atresia/stenosis, dysgenesis of sacrum, tethering of spinal cord, syringomyelia, hypoplasia of corpus callosum, cerebral ventriculomegaly and endocrine abnormalities. An autosomal recessive inheritance has been suggested. Disease data Klasyfikacja Malformation syndrome Synonimy Fryns microphthalmia syndrome Mikroftalmia z rozszczepem twarzy Zespół mikroftalmii Frynsa Microphthalmia with facial clefting Kod ORPHA 1104 Kod OMIM 600776 Kod ICD10 Q87.8 Kod ICD11 LD21.0 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl