Disease #04165 (Lichtenstein–Knorr syndrome)

Official abbreviation -
Name Lichtenstein–Knorr syndrome
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SLC9A1
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Disease features -
Remarks -
Date created 2014-12-23 22:06:25 +01:00 (CET)
Date last edited N/A


Individuals

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00027175 - PubMed: Guissart 2014 4-generation family, 3 affecteds (2F, M), unaffected heterozygous carrier parents - yes Turkey - - - - - Lichtenstein–Knorr syndrome see paper; early onset cerebellar ataxia, deafness SLC9A1 CATSPER4, CNKSR1, HSPG2, LAPTM5, SDC3, SERINC2, SLC9A1 7 3 Johan den Dunnen
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