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[X] neurofibromatosis

Go to external page http://purl.obolibrary.org/obo/MONDO_0021061

A hereditary neoplastic syndrome in which tumors grow in the nervous system. There are typically 3 main types recognized, but other forms with uncertain etiology exist. [ http://en.wikipedia.org/wiki/Neurofibromatosis NCIT:C6727 https://orcid.org/0000-0002-6601-2165 ]

Synonyms: type IV neurofibromatosis of riccardi acoustic neurofibromatosis von Reklinghausen disease neurofibromatosis Recklinghausen's neurofibromatosis peripheral Neurofibromatosis central Neurofibromatosis neurofibromatosis syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:D017253 (MONDO:equivalentTo)
  • NANDO:1200226 (https://orcid.org/0000-0003-0011-764X)
  • NCIT:C6727 (MONDO:equivalentTo)
  • EFO:0008514 (MONDO:equivalentTo)
  • MEDGEN:58149 (MONDO:equivalentTo)
  • ICDO:9540/1 (NCIT:C6727)
  • NANDO:1200225 (https://orcid.org/0000-0003-0011-764X)
  • NANDO:2201003 (https://orcid.org/0000-0003-0011-764X)
  • ICD9:237.70 (MONDO:i2s)
  • UMLS:C0162678 (MONDO:equivalentTo)
  • ICD9:237.7 (DOID:8712)
  • NANDO:1200227 (https://orcid.org/0000-0003-0011-764X)
  • GARD:10420 (MONDO:GARD)
  • SCTID:19133005 (MONDO:equivalentTo)
  • ICD9:237.71 (DOID:8712)
  • DOID:8712 (MONDO:equivalentTo)
  • ICD9:237.72 (DOID:8712)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, mondo_top_grouping_member, matrix_llm__txgnn_other, nord_rare, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, mondo_top_grouping_syndromic_disease, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, susceptibility_mondo, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease

exactMatch

http://linkedlifedata.com/resource/umls/id/C0162678

http://identifiers.org/medgen/58149

http://purl.obolibrary.org/obo/DOID_8712

http://identifiers.org/mesh/D017253

http://purl.obolibrary.org/obo/NCIT_C6727

http://www.ebi.ac.uk/efo/EFO_0008514

http://identifiers.org/snomedct/19133005

has narrow synonym

neurofibromatosis type IV

neurofibromatosis type 4

neurofibromatosis type 2

id

MONDO:0021061