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17827007: Cross syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
30111010 Cross syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
30112015 Oculocerebral-hypopigmentation syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
745175018 Cross syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3793253016 Oculocerebral hypopigmentation syndrome Cross type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3793254010 Kramer syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
30111010 Cross syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
30112015 Oculocerebral-hypopigmentation syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
30112015 Oculocerebral-hypopigmentation syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
30115018 Gingival fibromatosis, hypopigmentation, microphthalmia, oligophrenia AND athetosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
30116017 Hypopigmentation AND microphthalmia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
745175018 Cross syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
745175018 Cross syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3793253016 Oculocerebral hypopigmentation syndrome Cross type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3793254010 Kramer syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
557171000274115 Cross-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3431731001000115 Okulozerebrales Hypopigmentierungs-Syndrom Typ Cross de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5998901000241114 syndrome oculocérébral d'hypopigmentation de type Cross fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5998911000241111 syndrome de Cross fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5998901000241114 syndrome oculocérébral d'hypopigmentation de type Cross fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5998911000241111 syndrome de Cross fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
557171000274115 Cross-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3431731001000115 Okulozerebrales Hypopigmentierungs-Syndrom Typ Cross de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cross syndrome Is a anomalie congénitale de l'appareil respiratoire false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Tyrosinase-positive oculocutaneous albinism false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Microphthalmos false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Gingival fibromatosis false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Congenital anomaly of face false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Associated morphology Fibromatosis false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Associated morphology Fibromatosis false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Finding site Periodontal tissues structure false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Associated morphology Fibroepithelial hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Jaw region structure false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Cross syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Is a Congenital anomaly of face false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Finding site Eye structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Due to Disorder of tyrosine metabolism (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Associated morphology Hypertrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Associated morphology Fibromatosis false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Finding site œil entier false Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Cross syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Finding site œil entier false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 5
Cross syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 6
Cross syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 6
Cross syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 6
Cross syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cross syndrome Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 4
Cross syndrome Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Oculocutaneous albinism true Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cross syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Cross syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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