Disease #06235 (GADEVS (Gabriele-de Vries syndrome), OMIM:617557)

Official abbreviation GADEVS
Name Gabriele-de Vries syndrome
OMIM ID 617557
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene YY1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00457752 310897 - - M no Turkey - - - - - GADEVS Global developmental delay, Proptosis, Downslanted palpebral fissures, Macrocephaly, Neonatal respiratory distress, Single transverse palmar crease, Cafe-au-lait spot, Hemangioma, Dilation of Virchow-Robin spaces, Ventriculomegaly, Hydrocephalus, Prominent forehead, Thin upper lip vermilion YY1 YY1 1 1 Andreas Laner
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