Phenotypes for disease #05915 (TBHS (hypertelorism, Teebi type syndrome (TBHS)))

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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000335773 multiple congenital anomalies TBHS1 hypertelorism (HP:0000316); omphalocele (HP:0001539); bicornuate uterus (HP:0000813); congenital diaphragmatic hernia (HP:0000776) Isolated (sporadic) 7 days 00y08m 00y01m - Maria Elena García Paya 00446571
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