Disease #06952 (DELMNES (Delpire-McNeill syndrome), OMIM:619083)

Official abbreviation DELMNES
Name Delpire-McNeill syndrome
OMIM ID 619083
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 SLC12A2
Associated tissues -
Disease features -
Remarks -
Date created 2022-08-05 13:51:14 +02:00 (CEST)
Date last edited N/A


Individuals

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00414703 202459 - - M no Germany - - - - - DELMNES delayed speech and language development, abnormality outer ear, neurodevelopmental delay, autistic behavior SLC12A2 SLC12A2 1 1 Andreas Laner
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