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

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000001951 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 - - Isolated (sporadic) - - - - - Fowzan Alkuraya 00003131
0000001952 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 - - Isolated (sporadic) - - - - - Fowzan Alkuraya 00003133
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