Phenotypes for disease #01220 (CMPD (dysplasia, campomelic), OMIM:114290)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000045184 - - - Familial, autosomal dominant 14y 16y ? type 2 collagenopathy - Karina Silveira 00058589
0000274245 prenatal ultrasound abnormalities: Dysplastic sacrum, Micromelia, Hyperechogenic kidneys, Fetal cystic hygroma prenatal - Isolated (sporadic) - - - - - Andreas Laner 00380395
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