Disease #07036 (IDDHISD (intellectual developmental disorder with hypotonia, impaired speech, dysmorphic facies), OMIM:619556)

Official abbreviation IDDHISD
Name intellectual developmental disorder with hypotonia, impaired speech, dysmorphic facies
OMIM ID 619556
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene TNPO2
Associated tissues -
Disease features -
Remarks -
Date created 2023-10-23 16:49:47 +02:00 (CEST)
Date last edited N/A


Individuals

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00436147 263978 - - M ? Somalia - - - - - ID, IDDHISD Macrocephaly, Delayed speech and language development, Hypotonia, Neurodevelopmental delay TNPO2 TNPO2 1 1 Andreas Laner
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