Phenotype #0000359579

Individual ID 00474786
Associated disease ?
Diagnosis/Initial Feingold syndrome
Diagnosis/Definite FGLDS1
Phenotype details see paper; ..., birth weight/length 25–50th; OFC SD-4; postnatal growth retardation SD-2; micorcephaly SD-4; mild intellectual disability; no micrognatia; brachymesophalangy II/V; no toe syndactyly 2/3; toe syndactyly 4/5; oesophageal atresia; no duodenal atresia; renal hypoplasia; no congenital cardiac defect; no deafness; no asplenia
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2026-03-25 17:36:07 +01:00 (CET)
Date last edited N/A

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