JSON

congenital hydrocephalus

Go to external page http://purl.obolibrary.org/obo/MONDO_0016349

Hydrocephalus that is present at birth. [ NCIT:C98876 ]

Synonyms: congenital hydrocephalus

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:6682 (MONDO:GARD)
  • NCIT:C98876 (MONDO:equivalentTo)
  • UMLS:C0020256 (MONDO:equivalentTo)
  • MedDRA:10010506 (Orphanet:2185/e)
  • icd11.foundation:1878746673 (Orphanet:2185)
  • NANDO:2200822 (https://orcid.org/0000-0003-0011-764X)
  • MEDGEN:9336 (MONDO:equivalentTo)
  • Orphanet:2185 (MONDO:equivalentTo)
  • SCTID:47032000 (MONDO:equivalentTo)
  • OMIMPS:236600 (MONDO:equivalentTo)
  • ICD10CM:Q03 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, ordo_disorder, gard_rare, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_included, nord_rare, rare, orphanet_rare, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, ordo_malformation_syndrome, mondo_top_grouping_nervous_system_disorder, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_hereditary_disease

closeMatch

http://identifiers.org/meddra/10010506

exactMatch

http://www.orpha.net/ORDO/Orphanet_2185

http://identifiers.org/medgen/9336

http://identifiers.org/snomedct/47032000

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1878746673

http://purl.obolibrary.org/obo/NCIT_C98876

http://linkedlifedata.com/resource/umls/id/C0020256

https://omim.org/phenotypicSeries/PS236600

http://purl.bioontology.org/ontology/ICD10CM/Q03

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0015219

id

MONDO:0016349

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml

term tracker item

https://github.com/monarch-initiative/mondo/issues/4069