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722207000: Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5402854016 A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402855015 A rare syndromic mitochondrial disease characterised by exocrine pancreatic insufficiency, dyserythropoietic anaemia, and calvarial hyperostosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3331151010 Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331152015 Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331153013 Pancreatic insufficiency, dyserythropoietic anaemia, calvarial hyperostosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6455701000241110 syndrome de Shteyer fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6455711000241112 syndrome d'insuffisance pancréatique, anémie dysérythropoïétique et hyperostose de la voute crânienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6455721000241117 syndrome d'insuffisance pancréatique, anémie dysérythropoïétique et hyperostose de la voute du crâne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3440941001000119 Pankreasinsuffizienz - Anämie - Hyperostose 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
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Due to Decreased erythrocyte production true Inferred relationship Some 5
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Exocrine pancreatic insufficiency true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Metabolic bone disease true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Congenital dyserythropoietic anemia true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Cytochrome-c oxidase deficiency true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Dysostosis of bone of skull true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Connective tissue hereditary disorder false Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Digestive system hereditary disorder true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Finding site Erythrocyte (cell) true Inferred relationship Some 6
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Has definitional manifestation érythropénie false Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Associated morphology Congenital dysplasia false Inferred relationship Some 6
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Occurrence Congenital false Inferred relationship Some 6
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Finding site Structure of vault of skull (body structure) false Inferred relationship Some 6
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Occurrence Congenital true Inferred relationship Some 7
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Finding site Structure of exocrine pancreas false Inferred relationship Some 7
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Interprets Red blood cell count true Inferred relationship Some 4
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Has interpretation Below reference range true Inferred relationship Some 3
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Has interpretation Below reference range true Inferred relationship Some 4
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 3
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Occurrence Congenital true Inferred relationship Some 1
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Finding site Structure of exocrine pancreas true Inferred relationship Some 1
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Associated morphology Congenital dysplasia false Inferred relationship Some 2
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Finding site Structure of vault of skull (body structure) true Inferred relationship Some 2
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Occurrence Congenital true Inferred relationship Some 2
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Associated morphology Dysplasia true Inferred relationship Some 2
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Autosomal recessive hereditary disorder true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Hereditary disorder of endocrine system (disorder) true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Developmental hereditary disorder true Inferred relationship Some
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Finding site Bone structure of cranium true Inferred relationship Some 7
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Associated morphology Dysplasia true Inferred relationship Some 7
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 7
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. Is a Disorder of digestive system specific to fetus OR newborn true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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