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717771007: Cloverleaf skull with multiple congenital anomalies 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
5401588019 This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401589010 This newly described syndrome is characterised by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3310437018 Cloverleaf skull with multiple congenital anomalies syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310439015 Cloverleaf skull with multiple congenital anomalies syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
950861000172118 syndrome de crâne en trèfle-anomalies congénitales multiples fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3448091001000111 Kleeblattschädel - multiple kongenitale Anomalien 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
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Is a Longitudinal deficiency of limb true Inferred relationship Some
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Is a Autosomal recessive hereditary disorder true Inferred relationship Some
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Is a Cloverleaf skull syndrome true Inferred relationship Some
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Is a Connective tissue hereditary disorder false Inferred relationship Some
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital premature fusion false Inferred relationship Some 6
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital false Inferred relationship Some 6
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Joint structure of suture of skull false Inferred relationship Some 6
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital false Inferred relationship Some 7
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital abnormal fusion false Inferred relationship Some 8
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital false Inferred relationship Some 8
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of lambdoid suture of skull false Inferred relationship Some 8
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital abnormal fusion false Inferred relationship Some 9
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital false Inferred relationship Some 9
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of sagittal suture of skull false Inferred relationship Some 9
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital false Inferred relationship Some 10
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital false Inferred relationship Some 11
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital premature fusion false Inferred relationship Some 10
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Joint structure of suture of skull false Inferred relationship Some 10
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology anomalie du développement false Inferred relationship Some 11
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Face structure false Inferred relationship Some 11
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital abnormal fusion false Inferred relationship Some 7
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of coronal suture of skull false Inferred relationship Some 7
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Abnormally short growth (morphologic abnormality) false Inferred relationship Some 6
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Entire limb false Inferred relationship Some 6
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital true Inferred relationship Some 1
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital true Inferred relationship Some 2
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital true Inferred relationship Some 4
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital true Inferred relationship Some 5
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of sagittal suture of skull true Inferred relationship Some 4
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital abnormal fusion false Inferred relationship Some 4
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Occurrence Congenital true Inferred relationship Some 3
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Pathological process (attribute) Pathological developmental process false Inferred relationship Some 6
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital abnormal fusion false Inferred relationship Some 5
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Abnormally short growth (morphologic abnormality) true Inferred relationship Some 3
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Entire limb true Inferred relationship Some 3
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Face structure true Inferred relationship Some 2
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of lambdoid suture of skull false Inferred relationship Some 5
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of coronal suture of skull false Inferred relationship Some 1
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Is a Congenital deformity false Inferred relationship Some
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Is a Developmental hereditary disorder true Inferred relationship Some
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital premature fusion false Inferred relationship Some 1
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of lambdoid suture of skull false Inferred relationship Some 4
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital premature fusion false Inferred relationship Some 4
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Congenital premature fusion false Inferred relationship Some 5
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of sagittal suture of skull false Inferred relationship Some 5
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of lambdoid suture of skull true Inferred relationship Some 1
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Premature fusion true Inferred relationship Some 1
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Premature fusion true Inferred relationship Some 4
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Finding site Structure of coronal suture of skull true Inferred relationship Some 5
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. Associated morphology Premature fusion true Inferred relationship Some 5

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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