Phenotypes for disease #00865 (CACP (camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP)), OMIM:208250)

11 entries on 1 page. Showing entries 1 - 11.
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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     
0000084345 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106542
0000084347 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106544
0000084348 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106545
0000084349 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106546
0000084350 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106547
0000084351 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106548
0000084352 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106549
0000084353 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106550
0000084354 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106551
0000084356 - - - Familial, autosomal recessive - - - - - Saliha Yilmaz 00106552
0000357036 Arthrogryposis multiplex congenita Congenital arthrogryposis Camptodactyly-arthropathy-coxa vara-pericarditis syndrome Isolated (sporadic) - - - - - Camille Verebi 00472227
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