Phenotypes for disease #03937 (IHPRF1 (hypotonia, infantile, with psychomotor retardation and characteristic facies, type 1 (IHPRF-1)), OMIM:615419)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

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Owner     

Individual ID     
0000060521 Hypotonia, infantile, with psychomotor retardation and characteristic facies (OMIM:615419) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080952
0000274656 DD; ID; hypotonia, regression; dysmorphic facial features (Neurological) - NALCN channelopathies Familial - - - - - LOVD 00380803
0000300159 - - - Familial, autosomal recessive - - - - - Alaaeldin Fayez 00408029
0000324084 severe intellectual disability, developmental delay - - Familial, autosomal recessive - - - - - Marketa Wayhelova 00433661
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