Phenotype #0000339576

Individual ID 00450521
Associated disease LADD
Phenotype details esophageal atresia, dextrocardia, hypoplasia of the phalanges of the thumb, lacrimal gland aplasia, xerostomía, pulmonar hipoplasia, scoliosis, madelung deformity, dental caries, generalized periodontitis
Diagnosis/Initial VACTERL association
Inheritance Familial, autosomal dominant
Diagnosis/Definite LADD syndrome 3 and esophageal atresia
Age/Examination 00y ()
Age/Diagnosis 22y
Age/Onset 00y00m00d
Phenotype/Onset Congenital onset
Protein -
Owner name Maria Elena García Paya
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maria Elena García Paya
Date created 2024-05-30 10:12:20 +02:00 (CEST)
Date last edited 2024-05-31 10:22:13 +02:00 (CEST)

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