autosomal dominant nonsyndromic deafness

Summary
Synonym
  • autosomal dominant deafness
Definition
A nonsyndromic deafness characterized by an autosomal dominant inheritance mode.
Super Class
autosomal dominant disease nonsyndromic deafness
Disease Ontology
DOID:0050564
ORDO
OMIM
WikiPathways (from TogoID)
Related Genes
Displaying all 9 entries
Gene ID Gene Symbol Description Source
1301 COL11A1 collagen type XI alpha 1 chain
4131 MAP1B microtubule associated protein 1B
5298 PI4KB phosphatidylinositol 4-kinase beta
8295 TRRAP transformation/transcription domain associated protein
9984 THOC1 THO complex subunit 1
79977 GRHL2 grainyhead like transcription factor 2
80000 GREB1L GREB1 like retinoic acid receptor coactivator
84196 USP48 ubiquitin specific peptidase 48
284656 EPHA10 EPH receptor A10
Displaying all 5 entries
Gene ID Gene Symbol Description Source
11941 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2
12814 Col11a1 collagen, type XI, alpha 1
17755 Map1b microtubule-associated protein 1B
230735 Epha10 Eph receptor A10
252973 Grhl2 grainyhead like transcription factor 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
25654 Col11a1 collagen type XI alpha 1 chain
Displaying 1 entry
Gene ID Gene Symbol Description Source
5740544 futsch futsch
Displaying 1 entry
Gene ID Gene Symbol Description Source
173794 vab-1 Ephrin receptor 1

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Last updated: December 9, 2024