Disease #00040 (NSHL (non-syndromic hearing loss))

Official abbreviation NSHL
Name non-syndromic hearing loss
OMIM ID -
Inheritance -
Individuals reported having this disease 8
Phenotype entries for this disease 1
Associated with 2 genes GJB2, GJB6
Associated tissues -
Disease features -
Remarks -


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00000242 Siti Aishah Zainal et al. (2012) - Malaysia Malay Kelantan - - NSHL - GJB2 GJB2 13 1 Nuur Athirah Binti Mohd Daud
00000258 A Asma et al. (2011) - Malaysia - - - - NSHL - GJB2 GJB2 2 1 Nuur Athirah Binti Mohd Daud
00000259 A Asma et al. (2011) - Malaysia - - - - NSHL - GJB6 GJB6 2 1 Nuur Athirah Binti Mohd Daud
00000273 B H I Ruszymah et al. (2005) M Malaysia Malay - - - NSHL - GJB2 GJB2 3 1 Nuur Athirah Binti Mohd Daud
00000274 B H I Ruszymah et al. (2005) F Malaysia Malay - - - NSHL - GJB2 GJB2 1 1 Nuur Athirah Binti Mohd Daud
00000275 B H I Ruszymah et al. (2005) F Malaysia Chinese - - - NSHL - GJB2 GJB2 2 1 Nuur Athirah Binti Mohd Daud
00000276 B H I Ruszymah et al. (2005) M Malaysia Chinese - - - NSHL - GJB2 GJB2 2 1 Nuur Athirah Binti Mohd Daud
00000482 Z Siti Aishah et al. (2008) - Malaysia Malay - - - NSHL - GJB2 GJB2 3 1 Nuur Athirah Binti Mohd Daud
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