Disease #00103 (MRLIAF (mental retardation, language impairment, autistic features (MRLIAF)), OMIM:613670)

Official abbreviation MRLIAF
Name mental retardation, language impairment, autistic features (MRLIAF)
OMIM ID 613670
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 2
Associated with 1 gene FOXP1
Associated tissues -
Disease features -
Remarks -
Date created 2013-01-16 09:42:45 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00004296 - - - F ? Italy white - - - - MRLIAF - TBC1D7 TBC1D7 1 1 Alexandre Reymond
00080795 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - BCNS, MRLIAF Basal cell nevus syndrome (OMIM: 109400), Mental retardation with language impairment and with or without autistic features (OMIM: 613670) FOXP1, PTCH1 FOXP1, PTCH1 2 1 Daniel Trujillano
00401507 121P - - F no Spain - - - - - ID, MRLIAF - - FOXP1 1 1 Alejandro Brea-Fernández
00435255 260872 - - M no Germany - - - - - MRLIAF, RSTS Intellectual disability, Autistic behavior, Motor tics, Short stature, Neurodevelopmental delay, Tip-toe gait, 2-3 toe syndactyly, Abnormality of the face, Pes planus; mother and 3 brothers with syndactyly II and III bilateral CREBBP, FOXP1 CREBBP, FOXP1 2 1 Andreas Laner
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