Phenotypes for disease #05308 (del 3pterp25 (chromosome deletion syndrome 3pter-p25), OMIM:613792)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000086038 congenital heart defect, autistic, mental retardation; hypertelorism, ptosis, flat/broad nasal root, long philtrum, downturned corner mouth, low set ears, bilateral overlap 2nd/4th toes over 3rd/5th toes, hypotonic - - Isolated (sporadic) - 0d - - Johan den Dunnen 00108444
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