Phenotypes for disease #05182 (IHPRF2 (hypotonia, infantile, with psychomotor retardation and characteristic facies, type 2 (IHPRF-2)), OMIM:616801)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060623 Hypotonia, infantile, with psychomotor retardation and characteristic facies 2 (OMIM:616801) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081054
0000274657 DD; ID; hypotonia, dysmorphic facial features; failure to thrive (Neurological) - NALCN channelopathies Familial - - - - - LOVD 00380804
0000350385 Growth abnormality (HP:0001507); Dysphagia (HP:0002015); Delayed speech and language development (HP:0000750); Hypotonia (HP:0001252); Global developmental delay (HP:0001263); Seizure (HP:0001250) - - Familial, autosomal recessive - - - - - Mario Benvenuto 00464364
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