metaphyseal chondrodysplasia
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Jansen's metaphyseal chondrodysplasia — Classification and external resources ICD 9 756.9 OMIM 156400 DiseasesDB … Wikipedia
Schmid metaphyseal chondrodysplasia — Schmid metaphyseal chondrodysplasia. См. метафизарная хондродисплазия Шмида. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
Metaphyseal chondrodysplasia (McKusick type) — Also known as the cartilage hair hypoplasia syndrome, this is a genetic form of short limbed dwarfism with skeletal features that also include normal head, inability to fully extends the elbows, chest cage deformity, bow legs (genu varum), and… … Medical dictionary
Metaphyseal dysplasia — Classification and external resources ICD 10 Q78.5 ICD 9 756.9 … Wikipedia
Chondrodysplasia punctata — Classification and external resources ICD 10 Q77.3 DiseasesDB 32527 … Wikipedia
metaphyseal dysostosis — a skeletal abnormality in which the epiphyses are normal, or nearly so, and the metaphyseal tissues are replaced by masses of cartilage, producing interference with enchondral bone formation, and expansion and thinning of the metaphyseal cortices … Medical dictionary
Rhizomelic chondrodysplasia punctata — Classification and external resources ICD 10 Q77.3 ICD 9 277.86 … Wikipedia
Chondrodysplasia, metaphyseal (McKusick type) — Also known as cartilage hair hypoplasia syndrome, this is a specific genetic form of short limbed dwarfism with skeletal features that also include normal head, inability to fully extends the elbows, chest cage deformity, bow legs (genu varum),… … Medical dictionary
COL10A1 — Collagen, type X, alpha 1(Schmid metaphyseal chondrodysplasia), also known as COL10A1, is a human gene.cite web | title = Entrez Gene: COL10A1 collagen, type X, alpha 1(Schmid metaphyseal chondrodysplasia)| url =… … Wikipedia
Collagen, type X, alpha 1 — PDB rendering based on 1gr3 … Wikipedia
