Disease #06213 (NEDHILD;MRD40 (neurodevelopmental disorder with hypotonia, impaired language, dysmorphic features (MRD40)), OMIM:616579)

Official abbreviation NEDHILD;MRD40
Name neurodevelopmental disorder with hypotonia, impaired language, dysmorphic features (MRD40)
OMIM ID 616579
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 CHAMP1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2023-10-23 16:08:01 +02:00 (CEST)


Individuals

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00466217 342127 - - M no Bosnia and Herzegovina - - - - - NEDHILD;MRD40 Hypotonia, Delayed gross motor development, Delayed speech and language development, Astigmatism CHAMP1 CHAMP1 1 1 Andreas Laner
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