Syndrome with congenital phagocyte functional defect as a major feature
ORPHA:674648Congenital disorder of glycosylation with cardiac malformation as a major feature
ORPHA:371183Congenital disorder of glycosylation with deafness as a major feature
ORPHA:371212Congenital disorder of glycosylation with epilepsy as a major feature
ORPHA:371071Congenital disorder of glycosylation with nephropathy as a major feature
ORPHA:371207Congenital functional phagocyte defect
ORPHA:183681Congenital malformation of the eye with glaucoma as a major feature
ORPHA:98631Congenital myasthenic syndrome with glycosylation defect
ORPHA:353327Genetic congenital malformation of the eye with glaucoma as a major feature
ORPHA:525677Genetic syndrome with a central nervous system malformation as a major feature
ORPHA:269564Genetic syndrome with a cerebellar malformation as a major feature
ORPHA:269567Genetic syndrome with a Dandy-Walker malformation as a major feature
ORPHA:269570Genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature
ORPHA:269573Genetic syndrome with limb malformations as a major feature
ORPHA:404577Non-syndromic congenital phagocyte functional defect
ORPHA:674896Other syndrome with a central nervous system malformation as a major feature
ORPHA:269531Other syndrome with lissencephaly as a major feature
ORPHA:102010Rare disease with adrenal Cushing syndrome as a major feature
ORPHA:314749Syndrome with a central nervous system malformation as a major feature
ORPHA:108991Syndrome with a cerebellar malformation as a major feature
ORPHA:269523Syndrome with a Dandy-Walker malformation as a major feature
ORPHA:269546Syndrome with alpha-thalassemia as a major feature
ORPHA:232288Syndrome with congenital neutropenia as a major feature
ORPHA:331184Syndrome with corpus callosum agenesis/dysgenesis as a major feature
ORPHA:199639Syndrome with limb malformations as a major feature
ORPHA:109009Syndrome with microcephaly as a major feature
ORPHA:269528Syndrome with pulmonary hypertension as a major feature
ORPHA:275853