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File:Autosomal dominant - en.svg
From WikiMD's Food, Medicine & Wellness Encyclopedia
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 22:33, 5 October 2023 | | 738 × 1,260 (31 KB) | Andreyyshore | . |
File usage
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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
- Achondrogenesis
- Acromicric dysplasia
- 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
- Cardiofaciocutaneous syndrome
- Central core disease
- Cerebral cavernous malformation
- Char syndrome
- Combined hyperlipidemia
- Congenital contractural arachnodactyly
- Congenital dyserythropoietic anemia type 3
- Costello syndrome
- Cowden syndrome
- Cryopyrin-associated periodic syndrome
- Cystinuria
- DYT-TOR1A
- Deafness-lymphedema-leukemia syndrome
- Denys-Drash syndrome
- Diamond-Blackfan anemia
- Distal muscular dystrophy
- Familial atypical multiple mole melanoma syndrome
- Familial cold autoinflammatory syndrome
- Familial hypercholesterolemia
- Familial hypertrophic cardiomyopathy
- Familial isolated hyperparathyroidism
- Familial pulmonary arterial hypertension leucopenia and atrial septal defect
- Familial thoracic aortic aneurysm and dissection
- Familial transthyretin amyloidosis
- Focal task-specific dystonia
- Frasier syndrome
- Gingival fibromatosis with hypertrichosis
- Glucocorticoid remediable aldosteronism
- Gordon syndrome
- Gorlin Chaudhry Moss syndrome
- Hereditary amyloidosis
- Hereditary antithrombin deficiency
- Hereditary elliptocytosis
- Hereditary hemorrhagic telangiectasia
- Hereditary leiomyomatosis and renal cell cancer syndrome
- Hereditary paraganglioma-pheochromocytoma
- Juvenile osteoporosis
- KBG syndrome
- Kniest dysplasia
- Landau-Kleffner syndrome
- Li-Fraumeni syndrome
- Liddle syndrome
- Limb-girdle muscular dystrophy
- Lymphedema–distichiasis syndrome
- Lynch syndrome
- Melanoma, familial
- Metachondromatosis
- Metaphyseal chondrodysplasia Schmid type
- Milroy disease
- Monilethrix
- Multiple endocrine neoplasia type 1
- Myotonic dystrophy
- Nail-patella syndrome
- Neonatal Onset Multisystem Inflammatory disease
- Neurofibromatosis
- Neurofibromatosis type 1
- Nevoid basal cell carcinoma syndrome
- Osteopetrosis
- Paget disease of bone
- Paraganglioma and gastric stromal sarcoma
- Peutz-Jeghers syndrome
- Poland syndrome
- Porphyria cutanea tarda
- Progressive osseous heteroplasia
- Protein C deficiency
- Pyogenic arthritis, pyoderma gangrenosum and acne
- Renal coloboma syndrome
- Reticular pigmented anomaly of the flexures
- SHORT syndrome
- Severe congenital neutropenia
- Stormorken syndrome
- Supravalvular aortic stenosis
- Thanatophoric dysplasia
- Tietz syndrome
- Tuberous sclerosis
- Tumor necrosis factor receptor-associated periodic syndrome
- Variegate porphyria
- Von Hippel-Lindau disease
- Von Hippel–Lindau disease
- Von Willebrand's disease
- Waardenburg syndrome
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