File:X-linked dominant.svg
From WikiMD's medical encyclopedia
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Summary
| Description |
English: X-linked dominant inheritance scenarios for either the mother or father being affected |
| Date | |
| Source | Based off of File:Autosomal dominant - en.svg |
| Author |
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| Note | For use on syndromes in which an affected male might be expected to pass on the condition. If not, use
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| Other versions |
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Licensing
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File history
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 17:19, 21 January 2020 | | 1,525 × 1,283 (166 KB) | SUM1 | Vertically aligned legend boxes |
File usage
The following 21 pages use this file:
- 2-methyl-3-hydroxybutyric aciduria
- Aicardi syndrome
- Bazex–Dupré–Christol syndrome
- Beta-Propeller Protein-Associated Neurodegeneration
- Craniofrontonasal dysplasia
- Frontometaphyseal dysplasia
- Microphthalmia with linear skin defects syndrome
- Microphthalmia–dermal aplasia–sclerocornea syndrome
- Nance–Horan syndrome
- Phosphate diabetes
- Subcortical band heterotopia
- Terminal osseous dysplasia with pigmentary defects
- Wildervanck syndrome
- Woods Black Norbury syndrome
- X-linked cone-rod dystrophy, type 1
- X-linked dominant chondrodysplasia punctata 2
- X-linked dominant inheritance
- X-linked hypertrichosis
- X-linked hypophosphatemia
- X-linked intellectual disability, Najm type
- X-linked periventricular heterotopia
