
 Phenotype ID
|

 Phenotype details
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Protein
|

 Owner
|

 Individual ID
|
0000027313 |
no vestibular, visual, renal, or muscular involvement |
- |
- |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033915 |
0000027314 |
no vestibular, visual, renal, or muscular involvement |
- |
- |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033916 |
0000027315 |
no vestibular, visual, renal, or muscular involvement |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033917 |
0000027316 |
nonsyndromic deafness |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033918 |
0000027317 |
nonsyndromic deafness |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033919 |
0000027318 |
nonsyndromic deafness |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033920 |
0000027319 |
nonsyndromic deafness |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033921 |
0000034025 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00043744 |
0000034055 |
DFNA9 |
- |
- |
Familial, autosomal dominant |
48y |
- |
48y |
- |
- |
Han Sang Kim |
00043837 |
0000034056 |
DFNA9 |
- |
- |
Familial, autosomal dominant |
52y |
- |
52y |
- |
- |
Han Sang Kim |
00043836 |
0000041957 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Michel van Geel |
00055302 |
0000041958 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Michel van Geel |
00055303 |
0000041962 |
- |
- |
- |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Michel van Geel |
00055307 |
0000041963 |
- |
- |
- |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Michel van Geel |
00055308 |
0000041970 |
- |
- |
- |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Michel van Geel |
00055315 |
0000041977 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Michel van Geel |
00055322 |
0000041978 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Michel van Geel |
00055323 |
0000042002 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00055347 |
0000046744 |
DFNA-6/14/38; congenital NSHL, low-tone, U-shaped audiogram |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Zippi Brownstein |
00060255 |
0000060258 |
- |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Celia Zazo-Seco |
00037767 |
0000060259 |
see paper; ... |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Celia Zazo-Seco |
00037770 |
0000060261 |
- |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Mieke Wesdorp |
00079876 |
0000068353 |
- |
- |
- |
Familial, autosomal dominant |
49y |
03y |
03y? |
- |
- |
Hanno Bolz |
00088950 |
0000068355 |
- |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Hanno Bolz |
00088953 |
0000127218 |
see paper; ... |
- |
DFNA-50 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00154479 |
0000127219 |
see paper; ..., progressive, high-frequency hearing loss |
- |
DFNA-50 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00154480 |
0000128162 |
- |
Non-syndromic Deafness (DFN) |
DFNA-4B |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Barbara Vona |
00163025 |
0000128195 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163058 |
0000128196 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163059 |
0000128197 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163060 |
0000128198 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163061 |
0000128199 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163062 |
0000128200 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163063 |
0000128201 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163064 |
0000128202 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163065 |
0000128203 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163066 |
0000128204 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163067 |
0000128207 |
Cardiac hypertrophy and QT interval prolongation |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163070 |
0000128208 |
Cardiac hypertrophy and QT interval prolongation |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163071 |
0000128209 |
Cardiac hypertrophy and QT interval prolongation |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163072 |
0000128210 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163073 |
0000128211 |
Abnormal ECG |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163074 |
0000128212 |
Abnormal ECG |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163075 |
0000128213 |
Cardiac hypertrophy and QT interval prolongation |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163076 |
0000128214 |
Abnormal ECG |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163077 |
0000128215 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163078 |
0000128216 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163079 |
0000128217 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163080 |
0000128218 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163081 |
0000128219 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163082 |
0000128220 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163083 |
0000128221 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163084 |
0000128222 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163085 |
0000128223 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163086 |
0000128224 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163087 |
0000128225 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163088 |
0000128226 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163089 |
0000128227 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163090 |
0000128228 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163091 |
0000128229 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163092 |
0000128230 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163093 |
0000128231 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163094 |
0000128232 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163095 |
0000128233 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163096 |
0000128234 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163097 |
0000128235 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163098 |
0000128236 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163099 |
0000128237 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163100 |
0000128238 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163101 |
0000128239 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163102 |
0000128240 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163103 |
0000128243 |
Mild to moderate |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163106 |
0000128244 |
Mild and COCH mutation |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163107 |
0000128245 |
Moderate and COCH mutation |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163108 |
0000128246 |
Moderate |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163109 |
0000128247 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163110 |
0000128248 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163111 |
0000128249 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163112 |
0000128250 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163113 |
0000128251 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163114 |
0000128252 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163115 |
0000128258 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163121 |
0000128259 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163122 |
0000128260 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163123 |
0000128261 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163124 |
0000128262 |
- |
deafness, nonsyndromic (DFNA) |
DFNA-22 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163125 |
0000128326 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163189 |
0000128329 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163192 |
0000128330 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163193 |
0000128333 |
high frequency hearing loss |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Byung Yoon Choi |
00163196 |
0000128334 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163197 |
0000128336 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163199 |
0000128337 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163200 |
0000128338 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163201 |
0000128339 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163202 |
0000128340 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163203 |
0000128341 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163204 |
0000128344 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163207 |
0000128345 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163208 |
0000128346 |
- |
deafness, nonsyndromic (DFNA8/12) |
DFNA_12 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Anne-Françoise Roux |
00163209 |