File:Autosomal dominant - en.svg
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Summary
| Description |
English: Autosomal dominant - genetics (english version) Français : Transmission autosomique dominante avec un parent porteur (version anglaise) |
| Date | |
| Source |
Own work using:
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| Author |
Français : Domaina |
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Licensing
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File history
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 20:44, May 29, 2025 | | 738 × 1,260 (36 KB) | wikimediacommons>NotCarlJohnson1992 | File uploaded using svgtranslate tool (https://svgtranslate.toolforge.org/). Added translation for ka. |
File usage
The following 89 pages use this file:
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- Acro–dermato–ungual–lacrimal–tooth syndrome
- Adermatoglyphia
- Albright's hereditary osteodystrophy
- Aplasia cutis congenita
- Apolipoprotein B deficiency
- Autosomal dominant multiple pterygium syndrome
- Bannayan–Riley–Ruvalcaba syndrome
- Bart–Pumphrey syndrome
- Birt–Hogg–Dubé syndrome
- Camisa disease
- Cantú syndrome
- Combined hyperlipidemia
- Costello syndrome
- Cryopyrin-associated periodic syndrome
- Cyprus facial neuromusculoskeletal syndrome
- Darier's disease
- Dermatopathia pigmentosa reticularis
- DiGeorge syndrome
- Dunnigan familial partial lipodystrophy
- Ectrodactyly–ectodermal dysplasia–cleft syndrome
- Elastosis perforans serpiginosa
- Erythrokeratodermia variabilis
- Erythrokeratodermia with ataxia
- Familial Amyloidosis, Finnish Type
- Familial amyloid polyneuropathy
- Familial hypertriglyceridemia
- Focal palmoplantar and gingival keratosis
- Gardner's syndrome
- Gastrocutaneous syndrome
- Generalized lentiginosis
- Gingival fibromatosis with hypertrichosis
- Hairy palms and soles
- Hay–Wells syndrome
- Hereditary hemorrhagic telangiectasia
- Hereditary neurocutaneous angioma
- Hereditary progressive mucinous histiocytosis
- Hereditary sclerosing poikiloderma
- Hystrix-like ichthyosis–deafness syndrome
- Ichthyosis with confetti
- Inherited patterned lentiginosis
- Johnson–McMillin syndrome
- Keratolytic winter erythema
- Legius syndrome
- Lenz–Majewski syndrome
- Loeys–Dietz syndrome
- Lowry–MacLean syndrome
- Lymphedema praecox
- Lymphedema–distichiasis syndrome
- Marie Unna hereditary hypotrichosis
- Marshall syndrome
- Melkersson–Rosenthal syndrome
- Metaphyseal chondrodysplasia Schmid type
- Milroy's disease
- Monilethrix
- Muckle–Wells syndrome
- Multiple endocrine neoplasia type 1
- Multiple endocrine neoplasia type 2
- Naegeli–Franceschetti–Jadassohn syndrome
- Nager acrofacial dysostosis
- Nail–patella syndrome
- Neurofibromatosis
- Noonan syndrome
- Odonto–tricho–ungual–digital–palmar syndrome
- PAPA syndrome
- Pachyonychia congenita
- Parkes Weber syndrome
- Popliteal pterygium syndrome
- Porphyria cutanea tarda
- Proteus-like syndrome
- ROSAH syndrome
- Rombo syndrome
- Rubinstein–Taybi syndrome
- Say syndrome
- Scalp–ear–nipple syndrome
- Sneddon's syndrome
- TNF receptor associated periodic syndrome
- Tooth and nail syndrome
- Townes–Brocks syndrome
- Treacher Collins syndrome
- Triangular alopecia
- Tuberous sclerosis
- Ulnar–mammary syndrome
- Variegate porphyria
- WHIM syndrome
- Watson syndrome
- Westerhof syndrome
- White sponge nevus
