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734173003: Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3489209014 SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3489210016 SCARF syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3489211017 Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3489213019 Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403881010 A rare multiple congenital anomalies syndrome characterized by variable skeletal abnormalities (including craniostenosis, pectus carinatum, short sternum, joint hyperextensibility, and abnormal vertebrae), cutis laxa with excessive skin folds around the cheek, chin and neck, ambiguous genitalia with a micropenis and perineal hypospadia, an umbilical hernia, intellectual disability, premature aged appearance, and cardiac enlargement involving either the ventricles or atria. Facial dysmorphism is variable and can include multiple hair whorls, ptosis, high and broad nasal root, low set ears and small chin. Enamel hypocalcification, abnormal modeling of tubular bones, and reduced cutis laxa may become apparent later on. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403882015 A rare multiple congenital anomalies syndrome characterised by variable skeletal abnormalities (including craniostenosis, pectus carinatum, short sternum, joint hyperextensibility, and abnormal vertebrae), cutis laxa with excessive skin folds around the cheek, chin and neck, ambiguous genitalia with a micropenis and perineal hypospadia, an umbilical hernia, intellectual disability, premature aged appearance, and cardiac enlargement involving either the ventricles or atria. Facial dysmorphism is variable and can include multiple hair whorls, ptosis, high and broad nasal root, low set ears and small chin. Enamel hypocalcification, abnormal modelling of tubular bones, and reduced cutis laxa may become apparent later on. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3489209014 SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3489210016 SCARF syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3489211017 Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3489213019 Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3489212012 Syndrome with the association of skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, psychomotor retardation and facial abnormalities. So far, it has been described in two males (maternal first cousins). The mode of inheritance was suggested to be X-linked recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403881010 A rare multiple congenital anomalies syndrome characterized by variable skeletal abnormalities (including craniostenosis, pectus carinatum, short sternum, joint hyperextensibility, and abnormal vertebrae), cutis laxa with excessive skin folds around the cheek, chin and neck, ambiguous genitalia with a micropenis and perineal hypospadia, an umbilical hernia, intellectual disability, premature aged appearance, and cardiac enlargement involving either the ventricles or atria. Facial dysmorphism is variable and can include multiple hair whorls, ptosis, high and broad nasal root, low set ears and small chin. Enamel hypocalcification, abnormal modeling of tubular bones, and reduced cutis laxa may become apparent later on. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403882015 A rare multiple congenital anomalies syndrome characterised by variable skeletal abnormalities (including craniostenosis, pectus carinatum, short sternum, joint hyperextensibility, and abnormal vertebrae), cutis laxa with excessive skin folds around the cheek, chin and neck, ambiguous genitalia with a micropenis and perineal hypospadia, an umbilical hernia, intellectual disability, premature aged appearance, and cardiac enlargement involving either the ventricles or atria. Facial dysmorphism is variable and can include multiple hair whorls, ptosis, high and broad nasal root, low set ears and small chin. Enamel hypocalcification, abnormal modelling of tubular bones, and reduced cutis laxa may become apparent later on. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3420021001000110 SCARF-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3420021001000110 SCARF-Syndrom 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
SCARF syndrome Is a Ambiguous genitalia true Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a Metabolic bone disease (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a Craniosynostosis syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a retard mental false Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a Hereditary disorder of the integument (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a Reproductive system hereditary disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a Congenital/hereditary cutis laxa false Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 5
SCARF syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 6
SCARF syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 7
SCARF syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 7
SCARF syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 8
SCARF syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 5
SCARF syndrome Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier (core metadata concept) 6
SCARF syndrome Finding site Joint structure of suture of skull false Inferred relationship Existential restriction modifier (core metadata concept) 6
SCARF syndrome Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 5
SCARF syndrome Finding site External genitalia structure false Inferred relationship Existential restriction modifier (core metadata concept) 7
SCARF syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 8
SCARF syndrome Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
SCARF syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
SCARF syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
SCARF syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
SCARF syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
SCARF syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
SCARF syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
SCARF syndrome Finding site External genitalia structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
SCARF syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
SCARF syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
SCARF syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
SCARF syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
SCARF syndrome Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
SCARF syndrome Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier (core metadata concept) 4
SCARF syndrome Finding site Joint structure of suture of skull true Inferred relationship Existential restriction modifier (core metadata concept) 4
SCARF syndrome Finding site Connective tissue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Is a Musculoskeletal and connective tissue disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Finding site Connective tissue structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 5
SCARF syndrome Is a Inherited cutis laxa true Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 5
SCARF syndrome Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
SCARF syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 6
SCARF syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 6
SCARF syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 7
SCARF syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 7
SCARF syndrome Associated morphology Premature fusion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 4
SCARF syndrome Is a Disorder involving the integument of fetus OR newborn true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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