Disease #06100 (LIWAS (Liang-Wang syndrome), OMIM:618729)

Official abbreviation LIWAS
Name Liang-Wang syndrome
OMIM ID 618729
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene KCNMA1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00431297 204154 - - F no Germany - - - - - LIWAS Delayed speech and language development, Gait disturbance, Reduced tendon reflexes, Tremor, Gait ataxia, Abnormality of movement, Abnormality of the face KCNMA1 KCNMA1 1 1 Andreas Laner
00431887 213747 - - F no Germany - - - - - LIWAS - KCNMA1 - - 1 Andreas Laner
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