Category:Autosomal recessive disorders
Pages in this category should be moved to subcategories where applicable. This category may require frequent maintenance to avoid becoming too large. It should directly contain very few, if any, pages and should mainly contain subcategories. |
Wikimedia Commons has media related to Autosomal recessive diseases and disorders.
For more information on autosomal recessive inheritance, see the articles Autosome, Recessive gene and Dominance relationship.
Subcategories
This category has the following 3 subcategories, out of 5 total.
(previous page) (next page)S
T
- Tay–Sachs disease (4 P)
Pages in category "Autosomal recessive disorders"
The following 144 pages are in this category, out of approximately 436 total. This list may not reflect recent changes.
(previous page) (next page)N
- N-Acetylglutamate synthase deficiency
- Nakajo syndrome
- Nemaline myopathy
- Nephronophthisis
- Nestor-Guillermo progeria syndrome
- Netherton syndrome
- Neu–Laxova syndrome
- Neuronal ceroid lipofuscinosis
- Nevo syndrome
- Nezelof syndrome
- NGLY1 deficiency
- Niemann–Pick disease
- SMPD1-associated Niemann–Pick disease
- Niemann–Pick disease type C
- Nijmegen breakage syndrome
- North American Indian childhood cirrhosis
O
- Ochronosis
- Oculocutaneous albinism
- Oculocutaneous albinism type I
- Oculodentodigital dysplasia
- Odontoonychodermal dysplasia
- Oguchi disease
- Omenn syndrome
- Opsismodysplasia
- Ornithine aminotransferase deficiency
- Ornithine translocase deficiency
- Orotic aciduria
- Osteoporosis-pseudoglioma syndrome
- Otofaciocervical syndrome
- Otospondylomegaepiphyseal dysplasia
P
- Papillary fibroelastoma
- Papillon–Lefèvre syndrome
- Pascual-Castroviejo syndrome type 1
- Pendred syndrome
- Persistent Müllerian duct syndrome
- Phenylketonuria
- Pipecolic acidemia
- Pontocerebellar hypoplasia
- Porencephaly-cerebellar hypoplasia-internal malformations syndrome
- Posterior column ataxia-retinitis pigmentosa syndrome
- Primary ciliary dyskinesia
- Prolidase deficiency
- Propionic acidemia
- Pseudo-Hurler polydystrophy
- Pseudodominance
- Pseudoxanthoma elasticum
- Pterin-4 alpha-carbinolamine dehydratase deficiency
- Purine nucleoside phosphorylase deficiency
- Pycnodysostosis
- Pyknoachondrogenesis
- Pyruvate carboxylase deficiency
R
- Rabson–Mendenhall syndrome
- Raine syndrome
- RAPADILINO syndrome
- Reardon-Hall-Slaney syndrome
- Refsum disease
- Renal dysplasia-limb defects syndrome
- Renal–hepatic–pancreatic dysplasia
- Reproductive compensation
- Restrictive dermopathy
- Retinal cone dystrophy 3B
- Riboflavin-responsive exercise intolerance
- Roberts syndrome
- Rothmund–Thomson syndrome
- Rotor syndrome
- Ruijs-Aalfs syndrome
S
- Sabinas brittle hair syndrome
- Salla disease
- Salt and pepper syndrome
- Sandhoff disease
- Sanfilippo syndrome
- Sanjad–Sakati syndrome
- Santos–Mateus–Leal syndrome
- Sarcosinemia
- Schimke syndrome
- Schneckenbecken dysplasia
- Sengers syndrome
- Senior–Løken syndrome
- Severe congenital neutropenia
- Short-chain acyl-coenzyme A dehydrogenase deficiency
- Short-limb skeletal dysplasia with severe combined immunodeficiency
- Shwachman–Diamond syndrome
- Sickle cell disease
- Sickle cell trait
- Situs inversus
- Sly syndrome
- Smith–Lemli–Opitz syndrome
- SOFT syndrome
- Sonoda syndrome
- Spastic ataxia-corneal dystrophy syndrome
- SPG15 (disease)
- Spinal muscular atrophy
- Spinal muscular atrophy with progressive myoclonic epilepsy
- Sponastrime dysplasia
- Spondylo-meta-epiphyseal dysplasia
- Spondylo-ocular syndrome
- Spondyloenchondrodysplasia
- Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
- Spondylometaphyseal dysplasia with cone-rod dystrophy
- Sporadic late-onset nemaline myopathy
- STING-associated vasculopathy with onset in infancy
- Succinic semialdehyde dehydrogenase deficiency
- Sudden infant death with dysgenesis of the testes syndrome
- Sugarman syndrome
- Systemic primary carnitine deficiency
T
- Tangier disease
- Tay–Sachs disease
- Tel Hashomer camptodactyly syndrome
- Tetra-amelia syndrome
- Tetrahydrobiopterin deficiency
- Thalassemia
- Thiamine responsive megaloblastic anemia syndrome
- TRIANGLE disease
- Trichothiodystrophy
- Trimethylaminuria
- Triosephosphate isomerase deficiency
- Triple-A syndrome
- Tyrosine hydroxylase deficiency
- Tyrosinemia
- Tyrosinemia type I
- Tyrosinemia type II
- Tyrosinemia type III