Phenotype #0000350693

Individual ID 00464560
Associated disease MRXS35
Phenotype details fetal growth delay, microcephaly, microretrognathia, protruding ears, nasal bridge collapse and high-arched palate
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Ke Wu
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Ke Wu
Date created 2025-04-14 03:38:46 +02:00 (CEST)
Date last edited 2025-04-14 11:23:41 +02:00 (CEST)

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