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cardiofaciocutaneous syndrome 2

Go to external page http://purl.obolibrary.org/obo/MONDO_0014112

Any cardiofaciocutaneous syndrome in which the cause of the disease is a mutation in the KRAS gene. [ MONDO:patterns/disease_series_by_gene ]

Synonyms: cardiofaciocutaneous syndrome 2 cardiofaciocutaneous syndrome caused by mutation in kras cardiofaciocutaneous syndrome caused by mutation in KRAS kras cardiofaciocutaneous syndrome cardiofaciocutaneous syndrome type 2 KRAS cardiofaciocutaneous syndrome

This is just here as a test because I lose it

Term information

database cross reference
Subsets

matrix_llm__is_cancer_other, gard_rare, mondo_top_grouping_integumentary_system_disorder, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_included, nord_rare, matrix_txgnn_grouping_member, rare, mondo_top_grouping_cardiovascular_disorder, harrisons_view_musculoskeletal_system_disorder, mondo_top_grouping_syndromic_disease, harrisons_view_integumentary_system_disorder, matrix_llm__is_glucose_dysfunction_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_txgnn_grouping_cardiovascular_disorder, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cardiovascular_disorder, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis

abbreviation
CFC2 [ MONDO:Lexical ]

exactMatch

http://identifiers.org/medgen/815335

http://purl.obolibrary.org/obo/DOID_0111461

http://linkedlifedata.com/resource/umls/id/C3809005

https://omim.org/entry/615278

id

MONDO:0014112