Disease #07005 (NEDGS (neurodevelopmental disorder with poor growth and skeletal anomalies), OMIM:619880)

Official abbreviation NEDGS
Name neurodevelopmental disorder with poor growth and skeletal anomalies
OMIM ID 619880
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene PCDHGC4
Associated tissues -
Disease features -
Remarks -
Date created 2023-02-28 12:00:54 +01:00 (CET)
Date last edited N/A


Individuals

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00433030 - - - M yes Egypt - - - - - NEDGS - - PCDHGC4 1 1 Alaaeldin Fayez
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