recessive
155 results
1 - 100
recessive- recessive disorder
- autosomal recessive
- characteristic
- gene
- nephrolithiasis
- cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- porphyria
- anemia
- Turcot syndrome
- deafness
- blindness
- fundus
- peeling skin syndrome
- Imerslund syndrome
- nephronophthisis
- Pierson syndrome
- Werner syndrome
- deficiency
- Cohen syndrome
- DOOR syndrome
- parahemophilia
- Meier-Gorlin syndrome
- acidemia
- Jeune syndrome
- pyridoxine dependency
- neutropenia
- Pendred syndrome
- Rotor syndrome
- Seckel syndrome
- faciocardiomelic syndrome
- Gitelman syndrome
- Nezelof syndrome
- mutation
- Lowe syndrome
- Fountain syndrome
- Bloom syndrome
- Freeman-Sheldon syndrome
- Alstrom syndrome
- merosin
- Leber, Theodor
- Elejalde syndrome
- Stargardt disease
- leprechaunism
- glycogen storage disease
- lethal multiple pterygium syndrome
- mucolipidosis
- bare lymphocyte syndrome
- aciduria
- nanism
- allele
- MDC
- Sanjad-Sakati syndrome
- Rothmund-Thomson syndrome
- ARC syndrome
- sulfite oxidase deficiency
- Fukuyama disease
- Senior-Loken syndrome, Senior-L⊘ken syndrome
- oxalosis
- hereditary aceruloplasminemia
- polycythemia
- adrenoleukodystrophy
- Joubert syndrome
- sitosterolemia
- myeloperoxidase deficiency syndrome
- Lafora, Gonzalo R.
- fucosidosis
- Hartnup disease
- Unverricht disease, Unverricht syndrome
- Usher syndrome
- Sjogren-Larsson syndrome
- sialidosis
- methionine malabsorption syndrome
- albinism
- Miyoshi myopathy
- proteinosis
- Salla disease
- pseudoxanthoma
- Antley-Bixler syndrome
- Farber disease
- hyperekplexia, hyperexplexia
- neuroacanthosis
- hypoplasia
- mitochondrial disease
- ochronosis
- hyperplasia
- fetal akinesia deformation sequence
- immotile cilia syndrome
- Papillon-Lefèvre syndrome
- cystinosis
- Wolman disease
- Laurence-Moon-Biedl syndrome
- Becker muscular dystrophy