File:Autosomal recessive - en.svg
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Summary
Autosomal recessive inheritance (English version)
Licensing
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File history
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 05:01, 5 January 2017 | | 744 × 1,323 (174 KB) | 127.0.0.1 (talk) | Autosomal recessive inheritance (English version) |
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File usage
The following 45 pages link to this file:
- Autosomal recessive multiple epiphyseal dysplasia
- Bernard–Soulier syndrome
- CAMFAK syndrome
- Carbamoyl phosphate synthetase I deficiency
- Cenani–Lenz syndactylism
- Cerebrotendineous xanthomatosis
- Congenital muscular dystrophy
- Cystinuria
- Dihydropyrimidine dehydrogenase deficiency
- Dominance (genetics)
- Fibrochondrogenesis
- Fukuyama congenital muscular dystrophy
- GAPO syndrome
- Galloway Mowat syndrome
- Gunther disease
- Hyperlysinemia
- Hypervalinemia
- Ichthyosis prematurity syndrome
- Immunodeficiency–centromeric instability–facial anomalies syndrome
- Johanson–Blizzard syndrome
- Kostmann syndrome
- Laurence–Moon syndrome
- Leigh disease
- Leukocyte adhesion deficiency
- Limb-girdle muscular dystrophy
- Malonyl-CoA decarboxylase deficiency
- Marden–Walker syndrome
- Mulibrey nanism
- Niemann–Pick disease
- Nijmegen breakage syndrome
- Oguchi disease
- Opsismodysplasia
- Orotic aciduria
- Papillon–Lefèvre syndrome
- Perlman syndrome
- Progeroid syndromes
- Rothmund–Thomson syndrome
- Salla disease
- Sarcosinemia
- Short-chain acyl-coenzyme A dehydrogenase deficiency
- Spinal muscular atrophy
- Tetra-amelia syndrome
- Triosephosphate isomerase deficiency
- Ullrich congenital muscular dystrophy
- Woodhouse–Sakati syndrome
