Phenotypes for disease #06697 (FMD2 (Frontometaphyseal dysplasia 2), OMIM:617137)

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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000324874 - - Neurodevelopmental abnormality, Delayed speech and language development, Hypotonia, Joint hypermobility, Aganglionic megacolon, Synophrys, Hypertrichosis, Cryptorchidism, Umbilical hernia, Patent foramen ovale, Supravalvular aortic stenosis Unknown 03y - - - Andreas Laner 00434624
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