ICD-10: Q87.89

Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome Hirata disease Andersen-Tawil syndrome Danon disease white sponge nevus obsolete arachnodactyly Costello syndrome Donohue syndrome Walker-Warburg syndrome spondylocostal dysostosis congenital disorder of glycosylation type I congenital disorder of glycosylation type II glycogen storage disease XV muscular dystrophy-dystroglycanopathy type B1 primary congenital glaucoma ABCD syndrome triple-A syndrome acheiropody acrocapitofemoral dysplasia Aland Island eye disease Allan-Herndon-Dudley syndrome anauxetic dysplasia 1 obsolete anonychia congenita Baller-Gerold syndrome Bamforth-Lazarus syndrome pseudo-TORCH syndrome 1 Bannayan-Riley-Ruvalcaba syndrome Beare-Stevenson cutis gyrata syndrome Birt-Hogg-Dube syndrome blue cone monochromacy Borjeson-Forssman-Lehmann syndrome Bowen-Conradi syndrome brachydactyly-syndactyly syndrome Brooke-Spiegler syndrome neonatal period electroclinical syndrome methylmalonic aciduria and homocystinuria type cblD PSAT deficiency methylmalonic aciduria and homocystinuria type cblE congenital intrinsic factor deficiency Qazi Markouizos syndrome adenylosuccinase lyase deficiency ARC syndrome mitochondrial complex V (ATP synthase) deficiency nuclear type 1 Meckel syndrome Ogden syndrome achalasia microcephaly syndrome mucopolysaccharidosis IX Stargardt disease CHARGE syndrome Perrault syndrome Marshall-Smith syndrome pancreatic agenesis IMAGe syndrome phalanx chondroma spastic ataxia 5 succinic semialdehyde dehydrogenase deficiency Cogan-Reese syndrome acrofrontofacionasal dysostosis Baraitser-Winter syndrome Warburg micro syndrome pontocerebellar hypoplasia type 2C omodysplasia Ohdo syndrome Ohdo syndrome, SBBYS variant CEDNIK syndrome Vici syndrome Galloway-Mowat syndrome 1 orofaciodigital syndrome III orofaciodigital syndrome IV acrofacial dysostosis orofaciodigital syndrome XI orofaciodigital syndrome IX acrofacial dysostosis Rodriguez type chondrodysplasia Blomstrand type chromosome 10q23 deletion syndrome epithelial-stromal TGFBI dystrophy fibrochondrogenesis Schimke immuno-osseous dysplasia Warsaw breakage syndrome ablepharon macrostomia syndrome Kufor-Rakeb syndrome Ritscher-Schinzel syndrome Ritscher-Schinzel syndrome 1 Ritscher-Schinzel syndrome 2 3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 ulnar-mammary syndrome ethylmalonic encephalopathy chondrodysplasia-pseudohermaphroditism syndrome fetal encasement syndrome lethal congenital contracture syndrome 4 autosomal recessive Robinow syndrome congenital diarrhea hypomyelinating leukodystrophy 13 syndromic X-linked intellectual disability 14 obsolete Brooks-Wisniewski-Brown syndrome Griscelli syndrome type 2 Norrie disease Potocki-Lupski syndrome Bardet-Biedl syndrome 1