Disease #03672 (PMRED (psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED)), OMIM:614501)

Official abbreviation PMRED
Name psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED)
OMIM ID 614501
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 5
Associated with 1 gene SNIP1
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

3 entries on 1 page. Showing entries 1 - 3.
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00408983 12 PubMed: Puffenberger 2012 brother of 13; no patient number in publication, consecutive numbers given M - - Old Order Amish and Mennonite - - - - PMRED global developmental delay; intractable epilepsy; skull dysplasia - severe psychomotor delay, intractable seizures, bulbous nose, wide mouth and tongue, broad jaw with protuberant angles, short hands, short tapered fingers, and broad thumbs SNIP1 SNIP1 1 1 LOVD
00408984 13 PubMed: Puffenberger 2012 brother of 12; no patient number in publication, consecutive numbers given M - - Old Order Amish and Mennonite - - - - PMRED global developmental delay; intractable epilepsy; skull dysplasia - severe psychomotor delay, intractable seizures, bulbous nose, wide mouth and tongue, broad jaw with protuberant angles, short hands, short tapered fingers, and broad thumbs SNIP1 SNIP1 1 1 LOVD
00408985 14 PubMed: Puffenberger 2012 no patient number in publication, consecutive numbers given ? - - Old Order Amish and Mennonite - - - - PMRED global developmental delay; intractable epilepsy; skull dysplasia SNIP1 SNIP1 1 1 LOVD
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