ODDD

ODDD
oculodentodigital dysplasia.

Medical dictionary. 2011.

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  • oculodentodigital dysplasia — (ODDD), oculodento osseous dysplasia (ODOD) a rare hereditary condition caused by mutations in the GJA1 gene (locus: 6q21 q23.2), which encodes connexin 43, characterized by bilateral microphthalmos, abnormally small nose with anteverted nostrils …   Medical dictionary

  • Oculodentodigital syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = ICD10 = ICD9 = ICDO = OMIM = 164200 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Oculodentodigital syndrome (ODD syndrome) is an extremely rare genetic condition that typically… …   Wikipedia

  • Gap junction protein, alpha 1 — Gap junction protein, alpha 1, 43kDa PDB rendering based on 1r5s …   Wikipedia

  • Oculodentodigital dysplasia — Classification and external resources OMIM 164200 DiseasesDB 32980 Oculodentodigital syndrome (ODD syndrome) is an extremely rare genetic conditio …   Wikipedia

  • Connexin 43 — protein Name = gap junction protein, alpha 1, 43kDa (connexin 43) caption = width = HGNCid = 4274 Symbol = GJA1 AltSymbols = ODDD, GJAL EntrezGene = 2697 OMIM = 121014 RefSeq = NM 000165 UniProt = P17302 PDB = ECnumber = Chromosome = 6 Arm = q… …   Wikipedia

  • Hallermann–Streiff syndrome — Classification and external resources ICD 9 756.0 OMIM 234100 DiseasesDB …   Wikipedia

  • СИНДАКТИЛИЯ — мед. Синдактилия полное или частичное сращение соседних пальцев кисти или стопы. Наблюдают как генетически гетерогенное самостоятельное заболевание или в качестве компонента наследственных синдромов. В зависимости от степени вовлечения тканей… …   Справочник по болезням

  • Коннексин 43 — Структура коннексина 43. Обозначения …   Википедия

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