Disease #00263 (OFD9 (orofaciodigital syndrome, type IX (OFD-9)), OMIM:258865)

Official abbreviation OFD9
Name orofaciodigital syndrome, type IX (OFD-9)
OMIM ID 258865
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 0 genes -
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Disease features -
Remarks -
Date created 2013-10-31 13:51:12 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00003131 24285566-Fam2PatIV2 PubMed: Adly 2014, Journal: Adly 2014 4-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M yes Saudi Arabia Arab 00y03m - - - OFD9 severe midline cleft lip/palate, microcephaly, choanal atresia, severe coloboma, congenital heart disease (ASD, VSD), micropenis, abnormal inner ear structures; brain MRI pachygyria, absent corpus callosum; required oxygen supplementation untill 2m, severe respiratory tract infection; cardiorespiratory arrest , died at 3m SCLT1 SCLT1 1 1 Fowzan Alkuraya
00003133 24285566-Fam1PatIV1 PubMed: Adly 2014, Journal: Adly 2014 4-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M yes Saudi Arabia Arab 00y06m - - - OFD9 24w gestation-cleft lip, abnormal hands, small occipiofrontal circumference; birth-microcephaly, right microphthalmia, left anophthalmia, bilateral optic disc coloboma, severe midline cleft (lip/alveolus), hypertelorism, severe choanal stenosis, left hand post-axial polydactyly, ambiguous genitalia, ECG patent ductus arteriosus and ASD; further details see Adly, submitted; 6m-died cardiac arrest TBC1D32 TBC1D32 1 1 Fowzan Alkuraya
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