Synonyms: hypomaturation amelogenesis imperfecta
Term information
- Orphanet:100033 (MONDO:equivalentTo)
- UMLS:C0399372 (MONDO:equivalentTo)
- SCTID:109475005 (MONDO:equivalentTo)
- GARD:8349 (MONDO:GARD)
- MESH:C536606 (Orphanet:100033/e)
- ICD9:520.5 (MONDO:relatedTo)
- MEDGEN:97994 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, mondo_subtype, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, ordo_subtype_of_a_disorder, mondo_top_grouping_mouth_disorder, mondo_top_grouping_musculoskeletal_system_disorder, matrix_included, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_hereditary_disease, harrisons_view_musculoskeletal_system_disorder
http://www.orpha.net/ORDO/Orphanet_100033
http://identifiers.org/mesh/C536606
http://linkedlifedata.com/resource/umls/id/C0399372
http://identifiers.org/medgen/97994
http://identifiers.org/snomedct/109475005