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About not displaying Condition column on the biomarker list page as data is too big. #1267

Open sujeetvkulkarni opened 3 weeks ago

sujeetvkulkarni commented 3 weeks ago

In this case we will be not displaying the Condition column on the biomarker list page because as per @rykahsay list api text for condition is too big.

API: https://api.tst.glygen.org/biomarker/list id: 1e14c465c506a9fe2a55d1acc878199b condition value is given below,

 "condition": "prostate cancer (DOID:10283); NGP - new growth of prostate (DOID:10283); hereditary prostate cancer 
(DOID:10283); malignant tumor of the prostate (DOID:10283); prostate cancer, familial (DOID:10283); prostate neoplasm 
(DOID:10283); prostatic cancer (DOID:10283); prostatic neoplasm (DOID:10283); tumor of the prostate (DOID:10283); 
prostate cancer, hereditary, 9 (MONDO:0012597); prostate cancer, hereditary, type 9 (MONDO:0012597); HPC9 
(MONDO:0012597); prostate cancer, hereditary, 12 (MONDO:0012741); EHBP1 familial prostate cancer 
(MONDO:0012741); familial prostate cancer caused by mutation in EHBP1 (MONDO:0012741); prostate cancer, hereditary, 
type 12 (MONDO:0012741); HPC12 (MONDO:0012741); prostate cancer, hereditary, 5 (MONDO:0012244); prostate 
cancer, hereditary, type 5 (MONDO:0012244); HPC5 (MONDO:0012244); prostate cancer, hereditary, 3 
(MONDO:0012093); prostate cancer, hereditary, type 3 (MONDO:0012093); prostate cancer, susceptibility to, 3 
(MONDO:0012093); HPC3 (MONDO:0012093); prostate cancer, hereditary, 4 (MONDO:0012094); prostate cancer, 
hereditary, type 4 (MONDO:0012094); prostate cancer, susceptibility to, 4 (MONDO:0012094); HPC4 
(MONDO:0012094); prostate cancer, hereditary, on chromosome 7 (MONDO:0012094); prostate cancer, hereditary, 13 
(MONDO:0012758); MSMB familial prostate cancer (MONDO:0012758); familial prostate cancer caused by mutation in 
MSMB (MONDO:0012758); prostate cancer, hereditary, type 13 (MONDO:0012758); HPC13 (MONDO:0012758); prostate 
cancer, hereditary, 8 (MONDO:0011270); prostate cancer, hereditary, type 8 (MONDO:0011270); HPC8 
(MONDO:0011270); predisposing for prostate cancer (MONDO:0011270); prostate cancer, susceptibility to 
(MONDO:0011270); prostate cancer, hereditary, 6 (MONDO:0012300); prostate cancer, hereditary, type 6 
(MONDO:0012300); HPC6 (MONDO:0012300); prostate cancer, susceptibility to (MONDO:0012300); prostate cancer, 
hereditary, 10 (MONDO:0012620); HPC10 (MONDO:0012620); familial prostate carcinoma (MONDO:0023122); familial 
prostate cancer (MONDO:0023122); hereditary prostate cancer (MONDO:0023122); hereditary prostate carcinoma 
(MONDO:0023122); prostate cancer, autosomal dominant, somatic mutation (MONDO:0023122); prostate cancer, 
familial, susceptibility to, autosomal dominant, somatic mutation (MONDO:0023122); prostate cancer, somatic 
(MONDO:0023122); prostate cancer, susceptibility to, autosomal dominant, somatic mutation (MONDO:0023122); 
prostate cancer, familial (MONDO:0023122); prostate cancer, hereditary (MONDO:0023122); prostate cancer, hereditary,
 7 (MONDO:0012470); HPC7 (MONDO:0012470); prostate cancer aggressiveness (MONDO:0012470); prostate cancer, 
hereditary, 1 (MONDO:0011098); RNASEL familial prostate cancer (MONDO:0011098); familial prostate cancer caused by 
mutation in RNASEL (MONDO:0011098); prostate cancer 1 (MONDO:0011098); prostate cancer, hereditary, type 1 
(MONDO:0011098); HPC1 (MONDO:0011098); Prca1 (MONDO:0011098); prostate cancer, hereditary, 11 
(MONDO:0012768); HPC11 (MONDO:0012768); prostate cancer, hereditary, 14 (MONDO:0012769); HPC14 
(MONDO:0012769); prostate cancer, hereditary, 15 (MONDO:0012770); HPC15 (MONDO:0012770); prostate cancer, 
hereditary, X-linked 1 (MONDO:0010257); HPCX1 (MONDO:0010257); prostate cancer susceptibility, X-linked 
(MONDO:0010257); prostate cancer, hereditary, X-linked 2 (MONDO:0010405); HPCX2 (MONDO:0010405); Prostate 
cancer, hereditary, 12 (MIM:611868); Prostate cancer, hereditary, 13 (MIM:611928); Prostate cancer (MIM:176807); 
Prostate cancer, hereditary, 1 (MIM:601518); Prostate cancer, hereditary, 11 (MIM:611955)",
sujeetvkulkarni commented 1 week ago

Can you send only recommended name here for condition?