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Summary
| Description |
Autosomal recessive inheritance (English version)
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| Date | |
| Source | |
| Author | Domaina, Kashmiri and SUM1 |
| Other versions |
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Licensing
I, the copyright holder of this work, hereby publish it under the following license:
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File history
Click on a date/time to view the file as it appeared at that time.
| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 22:38, 5 October 2023 | | 738 × 1,283 (29 KB) | Andreyyshore | attempting to fix font size and spacing for newly-added languages |
| 22:34, 5 October 2023 |  | 738 × 1,283 (29 KB) | Andreyyshore | added Romanian and Turkish translations | |
| 02:15, 15 August 2023 |  | 738 × 1,283 (28 KB) | Parzeus | File uploaded using svgtranslate tool (https://svgtranslate.toolforge.org/). Added translation for pt-br. | |
| 12:18, 21 May 2023 |  | 738 × 1,283 (26 KB) | Kashmiri | Title in sans-serif, too | |
| 12:16, 21 May 2023 |  | 738 × 1,283 (26 KB) | Kashmiri | Code optimised | |
| 12:41, 25 October 2020 |  | 738 × 1,283 (27 KB) | Kashmiri | Further code cleanup | |
| 12:18, 25 October 2020 |  | 738 × 1,283 (27 KB) | Kashmiri | Code cleanup and optimisation. Replacing Arial typeface with generic (sans-serif) typeface for better display cross-OS. | |
| 03:47, 21 January 2020 |  | 738 × 1,283 (79 KB) | SUM1 | Further non-sex-linkage fix and fixed arrows | |
| 03:30, 21 January 2020 |  | 738 × 1,283 (79 KB) | SUM1 | Horizontally aligned child text | |
| 22:55, 20 January 2020 |  | 738 × 1,283 (79 KB) | SUM1 | Centred child text |
File usage
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.
- 2-Methylbutyryl-CoA dehydrogenase deficiency
- 6-Pyruvoyltetrahydropterin synthase deficiency
- AREDYLD syndrome
- Aagenaes syndrome
- Abdallat–Davis–Farrage syndrome
- Achondrogenesis type 1B
- Ackerman syndrome
- Adenosine deaminase deficiency
- Alström syndrome
- Analbuminaemia
- Aspartylglucosaminuria
- Asplenia with cardiovascular anomalies
- Autosomal recessive multiple epiphyseal dysplasia
- Bangstad syndrome
- Bardet–Biedl syndrome
- Bare lymphocyte syndrome
- Bare lymphocyte syndrome type II
- Bernard–Soulier syndrome
- Blount's disease
- Buphthalmos
- Carbamoyl phosphate synthetase I deficiency
- Cenani–Lenz syndactylism
- Cerebral palsy
- Cerebrotendineous xanthomatosis
- Chorea-acanthocytosis
- Chédiak–Higashi syndrome
- Cohen syndrome
- Congenital muscular dystrophy
- Costeff syndrome
- Cutis marmorata telangiectatica congenita
- Cystinuria
- DeSanctis–Cacchione syndrome
- Dihydropyrimidine dehydrogenase deficiency
- Dubowitz syndrome
- Factor VII deficiency
- Factor X deficiency
- Farber disease
- Fazio–Londe disease
- Fukuyama congenital muscular dystrophy
- GAPO syndrome
- Galactokinase deficiency
- Galactose epimerase deficiency
- Galloway–Mowat syndrome
- Glanzmann's thrombasthenia
- Glucocorticoid deficiency 1
- Glycogen storage disease type V
- Gray platelet syndrome
- Gunther disease
- Hereditary pyropoikilocytosis
- Hermansky–Pudlak syndrome
- Hyperlysinemia
- Hypoprothrombinemia
- Immunodeficiency–centromeric instability–facial anomalies syndrome
- Joubert syndrome
- Krabbe disease
- Laurence–Moon syndrome
- Leigh syndrome
- Letterer–Siwe disease
- Leukocyte adhesion deficiency
- Lipoid congenital adrenal hyperplasia
- Lipoprotein lipase deficiency
- Majewski's polydactyly syndrome
- Malonyl-CoA decarboxylase deficiency
- Maple syrup urine disease
- Mediastinal fibrosis
- Medium-chain acyl-coenzyme A dehydrogenase deficiency
- Metachromatic leukodystrophy
- Metaphyseal dysplasia
- Mismatch repair cancer syndrome
- Mulibrey nanism
- Neonatal hemochromatosis
- Nezelof syndrome
- Niemann–Pick disease
- Nijmegen breakage syndrome
- Oguchi disease
- Osteopetrosis
- Pacman dysplasia
- Papillon–Lefèvre syndrome
- Peters-plus syndrome
- Prolidase deficiency
- Pseudo-Hurler polydystrophy
- Purine nucleoside phosphorylase deficiency
- Raine syndrome
- Renal dysplasia-limb defects syndrome
- Rosselli–Gulienetti syndrome
- Rotor syndrome
- Sabinas brittle hair syndrome
- Salla disease
- Sandhoff disease
- Sarcosinemia
- Severe congenital neutropenia
- Short-chain acyl-coenzyme A dehydrogenase deficiency
- Sitosterolemia
- Spinal muscular atrophy
- Thrombotic thrombocytopenic purpura
- Thyroid dyshormonogenesis
- Triosephosphate isomerase deficiency
- Urofacial syndrome
- Usher syndrome
- Waardenburg syndrome
View more links to this file.
Global file usage
The following other wikis use this file:
- Usage on ar.wikipedia.org
- Usage on az.wikipedia.org
- Usage on bn.wikipedia.org
- Usage on bs.wikipedia.org
- Bardet–Biedlov sindrom
- Mišićna distrofija udovi-pojas
- MOPD II
- Frank–Ter Haarov sindrom
- Pravi hermafroditizam
- Nedostatak 5α-reduktaze
- Waardenburgov sindrom
- Nedostatak leukocitne adhezije
- Nedostatak adenozin-deaminaze
- Galaktozialidoza
- Nedostatak prolidaze
- Sindrom HUPRA
- Krvni antigen Vel
- Niemann–Pickova bolest
- Bruckov sindrom
- Usherov sindrom
- Nedostatak srednjelančane acil-koenzim A dehidrogenaze
- Alströmov sindrom
- Primarna hiperoksalurija
- Sensenbrennerin sindrom
- Sitosterolemija
- Leukoencefalopatija sa nestajanjem bijele mase
- Spinalna mišićna atrofija
- Zellwegerov sindrom
- Usage on cs.wikipedia.org
- Usage on el.wikipedia.org
- Usage on en.wikibooks.org
- Usage on es.wikipedia.org
- Usage on fa.wikipedia.org
View more global usage of this file.
