File:Autorecessive.svg
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 18:06, 18 September 2023 | | 1,350 × 1,580 (3 KB) | Puck04 | remake (by hand); path text --> <text> |
File usage
The following file is a duplicate of this file (more details):
- File:Autorecessive.svg from Wikimedia Commons
More than 100 pages use this file. The following list shows the first 100 pages that use this file only. A full list is available.
- 11-beta-hydroxylase deficiency
- 3-beta-hydroxysteroid dehydrogenase deficiency
- 3MC syndrome
- Acheiropodia
- Acrodermatitis enteropathica
- Acromesomelic dysplasia
- Afibrinogenemia
- Aldolase A deficiency
- Alström syndrome
- Anodontia
- Autoimmune polyglandular syndrome type 1
- Baller-Gerold syndrome
- Bardet-Biedl syndrome
- Bare lymphocyte syndrome 2
- Bartter syndrome
- Benign recurrent intrahepatic cholestasis 1
- Benign recurrent intrahepatic cholestasis 2
- Beta-ketothiolase deficiency
- Beta ketothiolase deficiency
- Biotinidase deficiency
- Bjornstad syndrome
- Bleeding disorder due to P2RY12 defect
- Bloom syndrome
- Boucher-Neuhäuser syndrome
- Bowen-Conradi syndrome
- Brody myopathy
- C1q deficiency
- Chondrodystrophy
- Chronic granulomatous disease
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Congenital generalized lipodystrophy
- Congenital thrombotic thrombocytopenic purpura
- Cystinosis
- Donohue syndrome
- Dysequilibrium syndrome
- Fanconi anemia
- Friedreich's ataxia
- Fryns syndrome
- Fucosidosis
- Fumarase deficiency
- GM1 gangliosidoses
- GRACILE syndrome
- Galactosemia
- Galactosialidosis
- Gaucher disease
- Gitelman syndrome
- Glanzmann thrombasthenia
- Glutathionuria
- Glycogen storage disease type 7
- Glycogen storage disease type II
- Harlequin ichthyosis
- Hemophagocytic lymphohistiocytosis
- Hepatoerythropoietic porphyria
- Hereditary fructose intolerance
- Hermansky-Pudlak syndrome
- Histidinemia
- Homocystinuria
- Hurler–Scheie syndrome
- Hyper-IgD syndrome
- Lafora disease
- Laron syndrome
- Lathosterolosis
- Leukodystrophy
- Lysosomal acid lipase deficiency
- Majeed syndrome
- Metachromatic leukodystrophy
- Mevalonate kinase deficiency
- Mitochondrial trifunctional protein deficiency
- Miyoshi myopathy
- Mucopolysaccharidosis type VII
- Multiple sulfatase deficiency
- N-Acetylglutamate synthase deficiency
- Neonatal adrenoleukodystrophy
- Nephronophthisis
- Nijmegen breakage syndrome
- Oculocutaneous albinism type 2
- Oculocutaneous albinism type 3
- Oculocutaneous albinism type I
- Pendred syndrome
- Prekallikrein deficiency
- Primary carnitine deficiency
- Propionic acidemia
- Pyruvate carboxylase deficiency
- Pyruvate kinase deficiency
- Rh deficiency syndrome
- Rhizomelic chondrodysplasia punctata
- Rosselli–Gulienetti syndrome
- Saccharopinuria
- Sanfilippo syndrome
- Scheie syndrome
- Sickle beta thalassemia
- Sickle cell anemia
- Sjögren–Larsson syndrome
- Tay-Sachs disease
- Thalassemia
- Thiamine responsive megaloblastic anemia syndrome
- Triosephosphate isomerase deficiency
- Waardenburg syndrome
- Wiedemann–Rautenstrauch syndrome
- Wilson disease
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