Microcephalic osteodysplastic primordial dwarfism type II
- Microcephalic osteodysplastic primordial dwarfism type II
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| Microcephalic osteodysplastic primordial dwarfism type II |
| Classification and external resources |
| OMIM |
210720 |
Microcephalic osteodysplastic primordial dwarfism type II (MOPD II) is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that MOPD, or a subtype of MOPD, affects less than 200,000 people in the US population and a form of dwarfism associated with brain and skeletal abnormalities.
It was characterized in 1982.[1]
It is associated with PCNT.[2]
See also
References
External links
| v · d · eCytoskeletal defects |
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| Microfilaments |
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| IF |
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| Microtubules |
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| Membrane |
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| Catenin |
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| Other |
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see also cytoskeletal proteins
B structural (perx, skel, cili, mito, nucl, sclr) · DNA/RNA/protein synthesis (drep, trfc, tscr, tltn) · membrane (icha, slcr, atpa, abct, othr) · transduction (iter, csrc, itra), trfk
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