Disease #05422 (MRFACD (mental retardation, distinctive facial features with/without cardiac defects), OMIM:616789)

Official abbreviation MRFACD
Name mental retardation, distinctive facial features with/without cardiac defects
OMIM ID 616789
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene MED13L
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2018-05-04 13:48:09 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00234320 - - - M no Italy - 19y - - - MRFACD - NLGN3, NLGN4X, NRXN1, PSMD12, TBR1, YWHAE, YY1, ZDHHC15, ZEB2 PSMD12 1 1 Pietro Palumbo
00399284 188556 - - F ? Germany - - - - - MRFACD Intellectual disability, Abnormal chromosome morphology, differential diagnosis initially down-syndrome MED13L MED13L 1 1 Andreas Laner
00424041 208666 - - M no Germany - - - - - MRFACD Epicanthus, Delayed speech and language development, Metatarsus adductus, Motor delay, Gliosis, Axial hypotonia, Broad-based gait, Global developmental delay MED13L MED13L 1 1 Andreas Laner
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