Diamond-Blackfan anemia 14 with mandibulofacial dysostosis
Duchenne muscular dystrophy +
ectodermal dysplasia 1 +
factor VIII deficiency +
Fanconi anemia complementation group B
FG syndrome +
frontometaphyseal dysplasia 1
A frontometaphyseal dysplasia characterized by generalized skeletal dysplasia, deafness, and urogenital defects that has_material_basis_in homozygous or hemizygous mutation in FLNA on chromosome Xq28. (DO)
frontometaphyseal dysplasia 2
Galloway-Mowat syndrome 2
glycogen storage disease IXA
glycogen storage disease IXD
glycogen storage disease VIII
hemophilia B
hereditary sensory neuropathy X-linked
hereditary spastic paraplegia 16
hereditary spastic paraplegia 2
hereditary spastic paraplegia 34
HRPT-related hyperuricemia
hypogonadotropic hypogonadism 1 with or without anosmia