Autosomal recessive pure spastic paraplegia
ORPHA:100982Autosomal recessive Robinow syndrome
ORPHA:1507Autosomal recessive severe congenital neutropenia
ORPHA:439849Autosomal recessive sideroblastic anemia
ORPHA:260305Autosomal recessive spastic ataxia
ORPHA:316240Autosomal recessive spastic ataxia of Charlevoix-Saguenay
ORPHA:98Autosomal recessive spastic ataxia with leukoencephalopathy
ORPHA:314603Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome
ORPHA:254343Autosomal recessive spondylocostal dysostosis
ORPHA:2311Autosomal recessive Stickler syndrome
ORPHA:250984Autosomal recessive syndromic cerebellar ataxia
ORPHA:98099Cartilage-hair hypoplasia
ORPHA:175Charcot-Marie-Tooth disease type 2B1
ORPHA:98856Charcot-Marie-Tooth disease type 2B2
ORPHA:101101Charcot-Marie-Tooth disease type 2H
ORPHA:101102Charcot-Marie-Tooth disease type 2T
ORPHA:495274Congenital hereditary endothelial dystrophy type II
ORPHA:293603Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
ORPHA:221145Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome
ORPHA:313772Exfoliative ichthyosis
ORPHA:289586Fukutin-related limb-girdle muscular dystrophy R13
ORPHA:206554Generalized pseudohypoaldosteronism type 1
ORPHA:171876Infantile nephronophthisis
ORPHA:93591OBSOLETE: Autosomal recessive hyper-IgE syndrome
ORPHA:169446OBSOLETE: Autosomal recessive optic atrophy
ORPHA:98675Osteopetrosis-hypogammaglobulinemia syndrome
ORPHA:178389