Global Variome shared LOVD

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Phenotype #0000350693 Individual ID 00464560 Associated disease MRXS35 Phenotype details see paper; ..., fetal growth delay, development delay, feeding difficulties, congenital laryngeal stridor, neonatal pneumonia, neonatal hypoglycemia, craniofacial anomalies, cryptorchidism Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite MRXS35 Age/Examination 00y02m (2 months) Age/Onset - Phenotype/Onset fetal growth delay Protein - Owner name Ke Wu Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Ke Wu Date created 2025-04-14 03:38:46 +02:00 (CEST) Date last edited 2026-08-28 15:42:17 +02:00 (CEST)

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