Phenotypes for disease #01709 (RCDP1 (chondrodysplasia punctata, rhizomelic, type 1 (RCDP-1)), OMIM:215100)

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     
0000104260 - - - Familial, autosomal recessive - - - - - Karina Silveira 00132076
0000274669 DD; short stature; bone malformation; failure to thrive (Neurological) - Rhizomelic chondrodysplasia punctata, type 1 Familial - - - - - LOVD 00380816
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