FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

716089008: Craniofacial digital and genital anomalies syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3304690010 Cranio-facio-digito-genital syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304691014 Harrod syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3304693012 Craniofacial digital and genital anomalies syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304694018 Craniofacial digital and genital anomalies syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401211019 A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of intellectual deficit, facial dysmorphism (a highly arched palate, pointed chin, and small mouth, hypotelorism, a long nose and large protruding ears), arachnodactyly, hypogenitalism (undescended testes and hypospadias) and failure to thrive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401212014 A rare multiple congenital anomalies/dysmorphic syndrome characterised by the association of intellectual deficit, facial dysmorphism (a highly arched palate, pointed chin, and small mouth, hypotelorism, a long nose and large protruding ears), arachnodactyly, hypogenitalism (undescended testes and hypospadias) and failure to thrive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Harrod syndrome Is a Arachnodactyly true Inferred relationship Some
Harrod syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Harrod syndrome Is a Mental retardation false Inferred relationship Some
Harrod syndrome Is a Congenital malformation of genital organs (disorder) true Inferred relationship Some
Harrod syndrome Is a Congenital abnormality of skull and face bones true Inferred relationship Some
Harrod syndrome Associated morphology Developmental anomaly false Inferred relationship Some 4
Harrod syndrome Occurrence Congenital true Inferred relationship Some 4
Harrod syndrome Finding site Genital structure false Inferred relationship Some 4
Harrod syndrome Occurrence Congenital false Inferred relationship Some 5
Harrod syndrome Occurrence Congenital false Inferred relationship Some 6
Harrod syndrome Associated morphology Developmental anomaly false Inferred relationship Some 7
Harrod syndrome Occurrence Congenital false Inferred relationship Some 7
Harrod syndrome Finding site Bone structure of head false Inferred relationship Some 7
Harrod syndrome Finding site Face structure true Inferred relationship Some 4
Harrod syndrome Associated morphology Abnormally long growth false Inferred relationship Some 5
Harrod syndrome Finding site Digit structure false Inferred relationship Some 5
Harrod syndrome Associated morphology Developmental anomaly false Inferred relationship Some 6
Harrod syndrome Finding site Face structure false Inferred relationship Some 6
Harrod syndrome Is a Intellectual disability true Inferred relationship Some
Harrod syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Harrod syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Harrod syndrome Occurrence Congenital true Inferred relationship Some 1
Harrod syndrome Associated morphology Abnormally long growth false Inferred relationship Some 3
Harrod syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Harrod syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Harrod syndrome Occurrence Congenital true Inferred relationship Some 3
Harrod syndrome Occurrence Congenital true Inferred relationship Some 2
Harrod syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Harrod syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Harrod syndrome Finding site Digit structure true Inferred relationship Some 3
Harrod syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
Harrod syndrome Finding site Bone structure of head true Inferred relationship Some 2
Harrod syndrome Finding site Genital structure true Inferred relationship Some 1
Harrod syndrome Associated morphology Abnormally long and slender growth true Inferred relationship Some 3
Harrod syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 5
Harrod syndrome Has interpretation Impaired true Inferred relationship Some 5
Harrod syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 6
Harrod syndrome Has interpretation Impaired true Inferred relationship Some 6

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

Back to Start