Phenotype #0000335773

Individual ID 00446571
Associated disease TBHS
Diagnosis/Initial multiple congenital anomalies
Diagnosis/Definite TBHS1
Phenotype details hypertelorism (HP:0000316); omphalocele (HP:0001539); bicornuate uterus (HP:0000813); congenital diaphragmatic hernia (HP:0000776)
Inheritance Isolated (sporadic)
Age/Examination 7 days
Age/Diagnosis 00y08m
Age/Onset 00y01m
Phenotype/Onset -
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 2024-01-18 09:12:15 +01:00 (CET)
Date last edited 2024-01-20 09:47:33 +01:00 (CET)

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