Disease #06379 (NEDCFSA (Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities), OMIM:618505)

Official abbreviation NEDCFSA
Name Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities
OMIM ID 618505
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene KDM6B
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00397651 189768 - - F ? (Saudi Arabia) - - - - - NEDCFSA Autism, Absent speech, Neurodevelopmental delay KDM6B KDM6B 2 1 Andreas Laner
00433507 241192 - - M no Germany - - - - - NEDCFSA Axial hypotonia, Strabismus, Neurodevelopmental delay, Hypotonia, Oral motor hypotonia, Epicanthus, Esodeviation, Hypomelanotic macule KDM6B KDM6B 1 1 Andreas Laner
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