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File:Autosomal dominant - en.svg
From WikiMD's Food, Medicine & Wellness Encyclopedia
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current | 22:33, 5 October 2023 | 738 × 1,260 (31 KB) | Andreyyshore | . |
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- File:Autosomal dominant - en.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.
- 22q11.2 deletion syndrome
- 7q11.23 duplication syndrome
- Acute intermittent porphyria
- Alagille Syndrome
- Bannayan-Riley-Ruvalcaba syndrome
- Benign familial neonatal epilepsy
- Birt-Hogg-Dube syndrome
- Boomerang dysplasia
- Brachydactyly type A1
- Brachydactyly type A2
- Brachydactyly type B
- Brachydactyly type C
- Brachydactyly type E
- Branchio-oto-renal syndrome
- Branchiootorenal syndrome
- Buschke Ollendorff syndrome
- CHARGE syndrome
- Camisa disease
- Cardiofaciocutaneous syndrome
- Cerebral cavernous malformation
- Combined hyperlipidemia
- Corneodermatoosseous syndrome
- Costello syndrome
- Cowden syndrome
- Cryopyrin-associated periodic syndrome
- Cystinuria
- Denys-Drash syndrome
- Diamond-Blackfan anemia
- Distal muscular dystrophy
- Erythrokeratodermia variabilis
- Familial atypical multiple mole melanoma syndrome
- Familial cold autoinflammatory syndrome
- Familial hypercholesterolemia
- Familial isolated hyperparathyroidism
- Frasier syndrome
- Hagemoser–Weinstein–Bresnick syndrome
- Hereditary elliptocytosis
- Hereditary leiomyomatosis and renal cell cancer syndrome
- Iridogoniodysgenesis, dominant type
- Keppen–Lubinsky syndrome
- Kniest dysplasia
- Kosaki overgrowth syndrome
- Lamb-Shaffer syndrome
- Landau-Kleffner syndrome
- Li-Fraumeni syndrome
- Liddle syndrome
- Li–Fraumeni syndrome
- Lymphedema–distichiasis syndrome
- Lynch syndrome
- Machado–Joseph disease
- Marshall syndrome
- McGillivray syndrome
- Metachondromatosis
- Metaphyseal chondrodysplasia Schmid type
- Muckle–Wells syndrome
- Multicentric carpotarsal osteolysis syndrome
- Multiple endocrine neoplasia type 1
- Myotonic dystrophy
- Naegeli–Franceschetti–Jadassohn syndrome
- Nail-patella syndrome
- Neurofibromatosis
- Neurofibromatosis type 1
- Nevoid basal cell carcinoma syndrome
- OSLAM syndrome
- Osteopetrosis
- PAPA syndrome
- PLAID syndrome
- Paget disease of bone
- Pashayan syndrome
- Peutz-Jeghers syndrome
- Poland syndrome
- Porphyria cutanea tarda
- Progressive osseous heteroplasia
- Pyogenic arthritis, pyoderma gangrenosum and acne
- Ramos-Arroyo syndrome
- Renal coloboma syndrome
- Reticular pigmented anomaly of the flexures
- Revesz syndrome
- Reynolds syndrome
- Rombo syndrome
- SHORT syndrome
- Say syndrome
- Schmitt Gillenwater Kelly syndrome
- Severe congenital neutropenia
- Shprintzen–Goldberg syndrome
- Singleton Merten syndrome
- Sneddon's syndrome
- Stickler syndrome
- Stormorken syndrome
- Supravalvular aortic stenosis
- Thanatophoric dysplasia
- Tietz syndrome
- Timothy syndrome
- Tuberous sclerosis
- Upington disease
- Variegate porphyria
- Von Hippel-Lindau disease
- Von Hippel–Lindau disease
- Von Willebrand's disease
- Waardenburg syndrome
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