Global Variome shared LOVD

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Phenotype #0000350385 Individual ID 00464364 Associated disease IHPRF2 Phenotype details 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) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Mario Benvenuto Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Mario Benvenuto Date created 2025-03-06 12:41:42 +01:00 (CET) Date last edited 2025-09-04 14:39:55 +02:00 (CEST)

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