File:Autorecessive.svg
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| Date/Time | Dimensions | User | Comment | |
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| current | 09:44, 22 July 2021 | 0 × 0 (75 KB) | Abdulkerim Yassin (talk | contribs) | |
| 12:58, 1 February 2016 | 512 × 599 (52 KB) | Jyostna Chouturi (talk | contribs) | Reverted to version as of 03:10, 8 September 2007 | |
| 12:58, 1 February 2016 | 1,350 × 1,580 (38 KB) | Jyostna Chouturi (talk | contribs) | ||
| 12:54, 1 February 2016 | 1,350 × 1,580 (38 KB) | Jyostna Chouturi (talk | contribs) | ||
| 03:10, 8 September 2007 | 512 × 599 (52 KB) | C Michael Gibson (talk | contribs) |
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File usage
The following 44 pages use this file:
- 2,8 dihydroxy-adenine urolithiasis
- 21-Hydroxylase Deficiency causes
- Abderhalden-Kaufmann-Lignac syndrome history and symptoms
- Ablepharon macrostomia syndrome
- Aceruloplasminemia
- Acheiropodia
- Alpha-mannosidosis
- Apparent mineralocorticoid excess
- Atransferrinemia
- Autosomal recessive
- Beta-mannosidosis
- Copper toxicosis
- Craniodiaphyseal dysplasia
- Dominance relationship
- Geroderma osteodysplastica
- Hartnup Disease overview
- Juvenile primary lateral sclerosis
- Lethal congenital contracture syndrome
- Lucey-Driscoll syndrome
- Meleda Disease
- Mevalonic aciduria
- Microvillous inclusion disease
- Microvillus inclusion disease
- Otospondylomegaepiphyseal dysplasia
- Papillon-Lefevre syndrome
- Pendred syndrome
- Phenylketonuria pathophysiology
- Price equation
- Progressive external ophthalmoplegia
- Purine nucleoside phosphorylase deficiency
- Recessive gene
- Rothmund-Thomson syndrome
- Sabinas brittle hair syndrome
- Sandhoff disease
- Sickle-cell disease pathophysiology
- Tay-Sachs disease
- Trimethylaminuria
- Tyrosinemia
- Very long-chain acyl-coenzyme A dehydrogenase deficiency
- Weissenbacher-Zweymüller syndrome
- Werner syndrome
- Xeroderma pigmentosum
- Yunis-Varon syndrome
- Zunich-Kaye syndrome
