Phenotypes for disease #04015 (LDS5;RNHF (Loeys-Dietz syndrome, type 5 (LDS-5, Rienhoff syndrome (RNHF))), OMIM:615582)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060433 Loeys-Dietz syndrome type 5 (OMIM:615582) - - Familial, autosomal dominant - - - - - Daniel Trujillano 00080864
0000333292 Macrocephaly, Tall stature, Pes planus, Delayed fine motor development, Expressive language delay, Cerebral white matter atrophy, Hypertelorism, Increased body weight - - Unknown 10y - - - - Andreas Laner 00444035
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