File:Autosomal dominant - en.svg
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 06:38, 22 December 2016 | | 738 × 1,283 (165 KB) | 127.0.0.1 (talk) | Autosomal dominant - genetics (ESPAÑOL version) |
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File usage
The following 70 pages link to this file:
- Albright's hereditary osteodystrophy
- Arakawa's syndrome II
- Axenfeld syndrome
- Bethlem myopathy
- Birt–Hogg–Dubé syndrome
- Boomerang dysplasia
- Branchio-oto-renal syndrome
- Central core disease
- Congenital stromal corneal dystrophy
- Currarino syndrome
- Darier's disease
- Dermatopathia pigmentosa reticularis
- DiGeorge syndrome
- Dominance (genetics)
- Endometrial cancer
- Familial atrial fibrillation
- Familial male-limited precocious puberty
- Flynn–Aird syndrome
- Gardner's syndrome
- Greig cephalopolysyndactyly syndrome
- Hajdu–Cheney syndrome
- Hawkinsinuria
- Hay–Wells syndrome
- Hereditary hemorrhagic telangiectasia
- Human genetics
- Hypoalphalipoproteinemia
- Jackson–Weiss syndrome
- Keratolytic winter erythema
- Kniest dysplasia
- Kostmann syndrome
- Liddle's syndrome
- Limb-girdle muscular dystrophy
- Marshall syndrome
- Medullary cystic kidney disease
- Mendelian traits in humans
- Metachondromatosis
- Monilethrix
- Multiple endocrine neoplasia type 2
- Myotonic dystrophy
- Naegeli–Franceschetti–Jadassohn syndrome
- Neuroacanthocytosis
- Noonan syndrome
- Pachyonychia congenita
- Pallister–Hall syndrome
- Papillorenal syndrome
- Pelger–Huet anomaly
- Platyspondylic lethal skeletal dysplasia, Torrance type
- Popliteal pterygium syndrome
- Porphyria cutanea tarda
- Romano–Ward syndrome
- Rubinstein–Taybi syndrome
- Short QT syndrome
- Spinocerebellar ataxia
- Spondyloepimetaphyseal dysplasia, Strudwick type
- Spondyloperipheral dysplasia
- Steatocystoma multiplex
- Stickler syndrome
- Tietz syndrome
- Timothy syndrome
- Transthyretin-related hereditary amyloidosis
- Treacher Collins syndrome
- Tuberous sclerosis
- Variegate porphyria
- Vitelliform macular dystrophy
- Von Hippel–Lindau disease
- Von Willebrand disease
- Waardenburg syndrome
- White sponge nevus
- Worth syndrome
- Zaspopathy
