Disease #07004 (NEDHFS (neurodevelopmental disorder with hypotonia, dysmorphic facies, skin abnormalities), OMIM:620191)

Official abbreviation NEDHFS
Name neurodevelopmental disorder with hypotonia, dysmorphic facies, skin abnormalities
OMIM ID 620191
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PGM2L1
Associated tissues -
Disease features -
Remarks -
Date created 2023-02-08 20:03:36 +01:00 (CET)
Date last edited N/A


Individuals

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00433668 - - - - - - - - - - - NEDHFS moderate intellectual disability, facial abnormality - CACNA1C, NFIB 2 1 Marketa Wayhelova
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