FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

4135001: 11p partial monosomy syndrome (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
8380016 11p partial monosomy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
778129019 11p partial monosomy syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
11p partial monosomy syndrome Is a Anomaly of chromosome pair 11 false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Is a Congenital aniridia false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Is a Nephroblastoma false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Is a Tumor of iris false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Finding site Iris structure false Inferred relationship Existential restriction modifier 4
11p partial monosomy syndrome Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 3
11p partial monosomy syndrome Associated morphology Monosomy false Inferred relationship Existential restriction modifier 1
11p partial monosomy syndrome Finding site Structure of nervous system false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 4
11p partial monosomy syndrome Associated morphology Nephroblastoma false Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Finding site Kidney structure false Inferred relationship Existential restriction modifier 1
11p partial monosomy syndrome Finding site Chromosome pair 11 false Inferred relationship Existential restriction modifier 3
11p partial monosomy syndrome Pathological process Malignant neoplastic process false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Finding site Iridial and/or ciliary structure false Inferred relationship Existential restriction modifier 3
11p partial monosomy syndrome Is a Malignant tumor of head and/or neck false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Is a Neoplasm of eye region false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Finding site Structure of parenchyma of kidney false Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Finding site Iridial and/or ciliary structure false Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 3
11p partial monosomy syndrome Is a Primary malignant neoplasm of retroperitoneum false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Finding site Chromosome pair 11 true Inferred relationship Existential restriction modifier 1
11p partial monosomy syndrome Associated morphology Monosomy false Inferred relationship Existential restriction modifier 4
11p partial monosomy syndrome Finding site Structure of parenchyma of kidney false Inferred relationship Existential restriction modifier 3
11p partial monosomy syndrome Associated morphology Nephroblastoma false Inferred relationship Existential restriction modifier 3
11p partial monosomy syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Finding site Iris structure false Inferred relationship Existential restriction modifier 1
11p partial monosomy syndrome Is a Hereditary disorder of the visual system false Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
11p partial monosomy syndrome Finding site Iris structure false Inferred relationship Existential restriction modifier 3
11p partial monosomy syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Finding site Chromosome pair 11 false Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 3
11p partial monosomy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
11p partial monosomy syndrome Associated morphology Absence false Inferred relationship Existential restriction modifier 1
11p partial monosomy syndrome Is a Deletion of part of chromosome 11 true Inferred relationship Existential restriction modifier
11p partial monosomy syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
11p partial monosomy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
11p partial monosomy syndrome Finding site Chromosome pair 11 true Inferred relationship Existential restriction modifier 2
11p partial monosomy syndrome Associated morphology Deletion of short arm true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Chromosome 11p11.2 deletion syndrome Is a True 11p partial monosomy syndrome Inferred relationship Existential restriction modifier
Chromosome 11p13 deletion syndrome Is a True 11p partial monosomy syndrome Inferred relationship Existential restriction modifier
11p15 deletion syndrome Is a True 11p partial monosomy syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start