nonsyndromic deafness (Q9079046)
auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms
Language:
Current Data About nonsyndromic deafness
(P31) (Q55789477)
(P248)
(P813) Saturday, July 28, 2018
(P5270) MONDO_0019497

(Q112193867)

(P279) (Q3505181)

(Q5325633)
(P248)
(P813) Monday, November 30, 2020
(P699) DOID:0050563

(Q55788460)
(P248)
(P813) Saturday, July 28, 2018
(P5270) MONDO_0019497

(P2293) (Q18037755)
(P248)
(P813) Wednesday, September 18, 2019
(P854) https://search.clinicalgenome.org/kb/gene-validity/3188ec93-954a-4daa-b99d-7c5fccad8e1a--2018-12-26T17:00:00

(Q18049583)
(P248)
(P813) Wednesday, September 18, 2019
(P854) https://search.clinicalgenome.org/kb/gene-validity/02c62d06-b496-4a48-a514-56a772fae071--2019-05-21T16:00:00

(Q18027461)
(P248)
(P813) Wednesday, September 18, 2019
(P854) https://search.clinicalgenome.org/kb/gene-validity/fce4988a-fb20-4f95-b73a-799c47b67e3b--2018-03-20T16:00:00

(Q18054763)
(P248)
(P813) Monday, September 14, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/a4dce399-9aeb-452e-a917-3603eb09d11f--2017-09-12T04:00:00

(Q17709277)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/db9f5d19-5ebc-4a1a-a4c3-79ff27f69a0e--2019-01-07T17:00:00

(Q18045544)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/f5799772-f233-4004-99a8-e6a0dddf0e8b--2018-05-22T04:00:00

(Q18035447)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/d4187cb6-182f-43fc-aeec-d27297c36bdb--2018-02-20T17:00:00

(Q18037280)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/17528cdb-97e0-4128-92de-9e419902aa62--2018-05-01T16:00:00

(Q17913983)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/998da390-3e32-4b80-a733-d64d87d5357b--2018-01-05T17:00:00

(Q18047246)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/7c63a581-ad69-4f18-b68b-d1b2cef5e699--2018-02-27T17:00:00

(Q5401842)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/03c875bb-70aa-4652-a7f2-35df1065165b--2018-04-24T16:00:00

(Q17917387)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/21c75059-bd7b-48ef-a828-28ffebe52ca0--2018-01-05T17:00:00

(Q18049724)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/e5feebe1-59a9-4e28-ad85-aec5cad6b54e--2017-08-22T16:00:00

(Q18056631)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/4becaf23-4b72-4dd1-a5aa-4deccbb394ea--2018-04-24T04:00:00

(Q18054855)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/e5e1a608-edc3-405c-805f-a7ed162c2bbc--2017-11-21T17:00:00

(Q18033856)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/88196c6d-4bd7-4aff-ba98-c7b4411c562d--2017-11-21T17:00:00

(Q18053573)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/8a029f02-3524-4932-9293-9c02304fdd2b--2018-04-24T16:00:00

(Q18049627)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/a35c0909-7546-465c-a069-47e901fce483--2018-05-08T04:00:00

(Q18052235)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/ba6df3f7-a000-401c-94d9-0dc5cb901f32--2018-08-29T19:16:31

(Q18046347)
(P248)
(P813) Monday, May 4, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/007697a5-2f83-40d0-b2ea-914e458a1452--2018-06-19T04:00:00

(Q18040062)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/2cf0898e-5e63-4327-9341-fdf26490beee--2017-11-21T17:00:00

(Q18029794)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/50d408fe-e298-4683-985c-57a37b30e273--2018-02-20T17:00:00

(Q14914027)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/598b33f0-cdad-4290-b6eb-f9c2304c7bb6--2018-03-19T16:00:00

(Q18051437)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/87661be2-f024-49bb-a60e-a906f7f113b7--2018-05-01T04:00:00

(Q18055453)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/0fac4fd4-d674-4017-a9a6-1d6793162c6b--2018-06-28T16:00:00

(Q18054103)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/28b962a1-8394-4366-8746-4b71a59cd60b--2018-01-05T17:00:00

(Q18058977)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/b3e304c3-33fd-41ec-81f9-1c0725a5549f--2017-12-19T05:00:00

(Q18030670)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/4ab4f4a3-757d-4de3-90e7-42a229c360a0--2018-01-05T17:00:00

(Q18030673)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/1476f1d9-7538-40bd-b602-b76781630cee--2017-11-21T17:00:00

(Q18031082)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/2cf494e5-7335-4e2a-8b50-75cf8412a9d0--2018-01-02T17:00:00

(Q18037581)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/29773bee-1f13-43f6-bda0-c5a646efccd7--2017-09-12T16:00:00

(Q18052497)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/977b98b7-00f4-4200-9b17-f37303889ab4--2017-12-19T05:00:00

(Q18031940)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/0c7395aa-89bb-40e2-a226-0500fef478bb--2018-09-12T15:56:22

(Q18049298)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/966d2fa1-5245-420d-9bf0-4a36aab29d74--2018-06-22T16:00:00

(Q18053904)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/b025a472-0a48-469c-a5f3-70df12ade334--2017-09-29T04:00:00

(Q18045709)
(P248)
(P813) Wednesday, December 9, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/ee13ba8c-7986-4e6c-8a39-4ee197ba4023--2017-08-22T16:00:00

(Q18040310)
(P248)
(P813) Monday, August 10, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/20de88d2-6681-4522-9e11-26cdf66a2c15--2020-02-06T17:00:00

(Q18046508)
(P248)
(P813) Tuesday, December 8, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/a2ca9952-b611-4e6f-bbf8-aa5175248d01--2020-05-01T16:00:00

(Q18053710)
(P248)
(P813) Monday, December 6, 2021
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_3ea7c7e0-dc56-4484-b2b6-5e3899d04013-2021-11-30T170000.000Z

(P2888) http://purl.obolibrary.org/obo/DOID_0050563
(P248)
(P813) Monday, November 30, 2020
(P699) DOID:0050563

http://identifiers.org/doid/DOID:0050563
(P248)
(P854) https://registry.identifiers.org/registry/doid

http://www.orpha.net/ORDO/Orphanet_87884

(P5008) (Q4099686)

other details
aliases nonsyndromic hearing loss
 nonsyndromic hereditary hearing loss
 Familial deafness
 Non-syndromic genetic deafness
 Isolated genetic deafness
description auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms

External Links
(P486) C580334
(P494) H90.5
(P699) DOID:0050563
(P1550) 87884
(P2892) C5680182
(P4229) H90.5
(P4317) 6410
(P5270) MONDO_0019497
(P6366) 2779163945
(P11143) Nonsyndromic deafness
(P11956) 0009076