Disease #01075 (MRXSLF (Lujan-Fryns syndrome), OMIM:309520)

Official abbreviation MRXSLF
Name Lujan-Fryns syndrome
OMIM ID 309520
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MED12
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00436391 269032 - - F no Germany - - - - - MRXSLF Neurodevelopmental delay, Absent speech, Hydrocephalus, Enlarged cisterna magna, Cerebellar atrophy, Patent foramen ovale, Patent ductus arteriosus, Hearing impairment, Intellectual disability, Autistic behavior, Strabismus, Dandy-Walker malformation MED12 MED12 1 1 Andreas Laner
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