pancreatic cancer, susceptibility to, 1
Go to external page http://purl.obolibrary.org/obo/MONDO_0011739
Any familial pancreatic carcinoma in which the cause of the disease is a mutation in the PALLD gene. [ MONDO:patterns/disease_series_by_gene ]
Synonyms: familial pancreatic carcinoma caused by mutation in PALLD PALLD familial pancreatic carcinoma pancreatic cancer, susceptibility to, type 1 pancreatic cancer, susceptibility to, 1
Term information
- OMIM:606856 (MONDO:equivalentTo)
- MEDGEN:339739 (MONDO:equivalentTo)
- UMLS:C1847351 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, predisposition, susceptibility_mondo, matrix_included, matrix_llm__tag_existing_treatment_other, inferred_rare, matrix_llm__anatomical_other, susceptibility_match, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, harrisons_view_cancer_or_benign_tumor, rare, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease, mondo_top_grouping_syndromic_disease
https://omim.org/entry/606856
http://identifiers.org/medgen/339739
http://linkedlifedata.com/resource/umls/id/C1847351
Term relations
- inherited disease susceptibility and has material basis in germline mutation in some PALLD and predisposes towards some [X] malignant pancreatic neoplasm