238855000: Hereditary camptodactyly (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Deformity (finding)\Deformity of limb (finding)\Camptodactyly\Hereditary camptodactyly (disorder)
\Deformity (finding)\Congenital deformity (disorder)\Congenital deformity of musculoskeletal system (disorder)\Camptodactyly\Hereditary camptodactyly (disorder)

\Finding of limb structure (finding)\Deformity of limb (finding)\Camptodactyly\Hereditary camptodactyly (disorder)
\Finding of limb structure (finding)\Disorder of limb\Disorder of digit\Congenital anomaly of digit\Congenital abnormal shape of digit\Camptodactyly\Hereditary camptodactyly (disorder)
\Finding of limb structure (finding)\Disorder of limb\Congenital anomaly of limb\Congenital anomaly of digit\Congenital abnormal shape of digit\Camptodactyly\Hereditary camptodactyly (disorder)

\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\...

\Hereditary disorder of musculoskeletal system\Hereditary camptodactyly (disorder)

\Congenital anomaly of musculoskeletal system\Congenital deformity of musculoskeletal system (disorder)\Camptodactyly\Hereditary camptodactyly (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Hereditary camptodactyly (disorder)
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Hereditary camptodactyly (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary camptodactyly (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital deformity (disorder)\Congenital deformity of musculoskeletal system (disorder)\Camptodactyly\Hereditary camptodactyly (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital deformity of musculoskeletal system (disorder)\Camptodactyly\Hereditary camptodactyly (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit\Congenital abnormal shape of digit\Camptodactyly\Hereditary camptodactyly (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Hereditary camptodactyly (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Hereditary disorder of musculoskeletal system\Hereditary camptodactyly (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital deformity of musculoskeletal system (disorder)\Camptodactyly\Hereditary camptodactyly (disorder)
\Disease\Disorder of limb\Disorder of digit\Congenital anomaly of digit\Congenital abnormal shape of digit\Camptodactyly\Hereditary camptodactyly (disorder)
\Disease\Disorder of limb\Congenital anomaly of limb\Congenital anomaly of digit\Congenital abnormal shape of digit\Camptodactyly\Hereditary camptodactyly (disorder)
\Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Hereditary camptodactyly (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital deformity (disorder)\Congenital deformity of musculoskeletal system (disorder)\Camptodactyly\Hereditary camptodactyly (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital deformity of musculoskeletal system (disorder)\Camptodactyly\Hereditary camptodactyly (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit\Congenital abnormal shape of digit\Camptodactyly\Hereditary camptodactyly (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary camptodactyly (disorder)	Is a	Palmar and plantar fibromatosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Finding site	Structure of fascia of hand (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Finding site	structure d'une aponévrose plantaire	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary camptodactyly (disorder)	Associated morphology	Fibromatosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary camptodactyly (disorder)	Finding site	Structure of soft tissue (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Associated morphology	Fibromatosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary camptodactyly (disorder)	Finding site	Palmar aponeurosis structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Finding site	Palm (region) structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary camptodactyly (disorder)	Associated morphology	Contracture	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Associated morphology	Fibromatosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary camptodactyly (disorder)	Is a	Superficial fibromatosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Finding site	Structure of musculoskeletal system	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary camptodactyly (disorder)	Finding site	Connective tissue structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Finding site	Structure of musculoskeletal system	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary camptodactyly (disorder)	Associated morphology	Fibromatosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary camptodactyly (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Is a	Camptodactyly	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary camptodactyly (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary camptodactyly (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary camptodactyly (disorder)	Associated morphology	Fixed flexion deformity (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary camptodactyly (disorder)	Finding site	Musculoskeletal system structure of digit (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary camptodactyly (disorder)	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Camptobrachydactyly (disorder)	Is a	True	Hereditary camptodactyly (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Camptodactyly taurinuria syndrome (disorder)	Is a	True	Hereditary camptodactyly (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
357976017	Hereditary camptodactyly	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
627792014	Hereditary camptodactyly (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
357976017	Hereditary camptodactyly	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
357976017	Hereditary camptodactyly	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
627792014	Hereditary camptodactyly (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
627792014	Hereditary camptodactyly (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5025891000241117	camptodactylie héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5025891000241117	camptodactylie héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module