📂 الأمراض
autosomal recessive nonsyndromic deafness 31 — التعريف
Otozomal Resesif Sendromik Olmayan Sağırlık 31 / autosomal recessive nonsyndromic deafness 31
والميراث العادم الحيواني هو اضطرابات سمعية تظهر أباً يُنظر إليه وحده بفقدان السمع (لا يقترن بنتائج مرسلة). This condition, also known as DFNB31, is often characterized by irradiating, non-compressive or slow-end sensor hearing loss. The disease develops the result of mutations in genes that play role in the structure of hair cells in the inner ear and often leads to moderate to advanced hearing loss.
الأسئلة الشائعة
❓ ما هو Otozomal Resesif Sendromik Olmayan Sağırlık 31؟
Otozomal Resesif Sendromik Olmayan Sağırlık 31; والميراث العادم الحيواني هو اضطرابات سمعية تظهر أباً يُنظر إليه وحده بفقدان السمع (لا يقترن بنتائج مرسلة). This condition, also known as DFNB31, is often characterized by irradiating, non-compressive or slow-end sensor hearing loss. The disease develops the result of mutations in genes that play role in the structure of hair cells in the inner ear and often leads to moderate to advanced hearing loss.
❓ ما معنى autosomal recessive nonsyndromic deafness 31 بالتركية؟
المعادل التركي لـ "autosomal recessive nonsyndromic deafness 31" هو Otozomal Resesif Sendromik Olmayan Sağırlık 31.
❓ ما هو المجال الطبي الذي يتعلق بـ Otozomal Resesif Sendromik Olmayan Sağırlık 31؟
هذا المصطلح ينتمي إلى فئة الأمراض.