Disease #06047 (LIS9 (Lissencephaly 9 with complex brainstem malformation), OMIM:618325)

Official abbreviation LIS9
Name Lissencephaly 9 with complex brainstem malformation
OMIM ID 618325
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MACF1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00466413 - Pending - M - France - - - - - LIS9 Short stature * Skeletal muscle atrophy * Kyphosis * Dry skin - BBS10, MACF1 2 1 Camille Verebi
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