Phenotypes for disease #00074 (NPHS1 (nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF))), OMIM:256300)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000016802 - Familial, autosomal recessive - - - - - - - Elisabet Ars Criach 00017906
0000016803 - Familial, autosomal recessive - - - - - - - Elisabet Ars Criach 00017907
0000017691 - Familial, autosomal recessive - - - - - - - Elisabet Ars Criach 00019917
0000232058 - Familial, autosomal recessive - - - - - - - Sha Hong 00306210
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