17144009: Fibrochondrogenesis (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Chondrodysplasia\Fibrochondrogenesis
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Fibrochondrogenesis
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Chondrodysplasia\Fibrochondrogenesis
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Chondrodysplasia\Fibrochondrogenesis
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Chondrodysplasia\Fibrochondrogenesis
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Chondrodysplasia\Fibrochondrogenesis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Fibrochondrogenesis
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Fibrochondrogenesis
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Fibrochondrogenesis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Fibrochondrogenesis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Fibrochondrogenesis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Chondrodysplasia\Fibrochondrogenesis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Chondrodysplasia\Fibrochondrogenesis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Chondrodysplasia\Fibrochondrogenesis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Chondrodysplasia\Fibrochondrogenesis
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Chondrodysplasia\Fibrochondrogenesis
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Chondrodysplasia\Fibrochondrogenesis
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Chondrodysplasia\Fibrochondrogenesis
\Disease\Developmental disorder\Developmental hereditary disorder\Fibrochondrogenesis
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Chondrodysplasia\Fibrochondrogenesis
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Chondrodysplasia\Fibrochondrogenesis

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

28994014 Fibrochondrogenesis en Synonym Active Entire term case insensitive SNOMED CT core module
744305018 Fibrochondrogenesis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Fibrochondrogenesis	Is a	Metatropic dysplasia	false	Inferred relationship	Existential restriction modifier
Fibrochondrogenesis	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Fibrochondrogenesis	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier	1
Fibrochondrogenesis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Fibrochondrogenesis	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Fibrochondrogenesis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Fibrochondrogenesis	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier
Fibrochondrogenesis	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	1
Fibrochondrogenesis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Fibrochondrogenesis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Fibrochondrogenesis	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Fibrochondrogenesis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	2
Fibrochondrogenesis	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Fibrochondrogenesis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Fibrochondrogenesis	Is a	Autosomal hereditary disorder	true	Inferred relationship	Existential restriction modifier
Fibrochondrogenesis	Is a	Chondrodysplasia	true	Inferred relationship	Existential restriction modifier
Fibrochondrogenesis	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Fibrochondrogenesis	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Short rib-polydactyly syndrome, non-Majewski type	Is a	False	Fibrochondrogenesis	Inferred relationship	Existential restriction modifier
Short rib-polydactyly syndrome, Majewski type	Is a	False	Fibrochondrogenesis	Inferred relationship	Existential restriction modifier
Dyggve-Melchior-Clausen syndrome	Is a	False	Fibrochondrogenesis	Inferred relationship	Existential restriction modifier
Short rib-polydactyly syndrome, Majewski type	Is a	False	Fibrochondrogenesis	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
28994014	Fibrochondrogenesis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
744305018	Fibrochondrogenesis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module