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733466005: Camptodactyly taurinuria syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3499487014 Camptodactyly taurinuria syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3499488016 Camptodactyly taurinuria syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3499489012 Familial streblodactyly with amino-aciduria en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Camptodactyly taurinuria syndrome Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Camptodactyly false Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Congenital anomaly of musculoskeletal system false Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Congenital abnormal shape of digit false Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Congenital deformity false Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Finding of musculoskeletal structure of finger false Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Inherited aminoaciduria true Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Associated morphology Congenital flexion deformity false Inferred relationship Existential restriction modifier 2
Camptodactyly taurinuria syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Camptodactyly taurinuria syndrome Finding site Musculoskeletal structure of finger false Inferred relationship Existential restriction modifier 2
Camptodactyly taurinuria syndrome Finding site Musculoskeletal structure of finger true Inferred relationship Existential restriction modifier 1
Camptodactyly taurinuria syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Camptodactyly taurinuria syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Camptodactyly taurinuria syndrome Associated morphology Flexion deformity false Inferred relationship Existential restriction modifier 1
Camptodactyly taurinuria syndrome Is a Congenital anomaly of finger false Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Associated morphology Fixed flexion deformity true Inferred relationship Existential restriction modifier 1
Camptodactyly taurinuria syndrome Is a Flexion deformity of hand false Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Hereditary camptodactyly true Inferred relationship Existential restriction modifier
Camptodactyly taurinuria syndrome Is a Camptodactyly of finger true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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