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719395001: Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3316198014 Microcephaly faciocardioskeletal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3316199018 Hadziselimovic syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3316201016 Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3316202011 Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5402083017 Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type is a rare syndrome with cardiac malformations, characterized by prenatal-onset growth retardation (low birth weight and short stature), hypotonia, developmental delay and intellectual disability associated with microcephaly and craniofacial (low anterior hairline, hypotelorism, thick lips with carp-shaped mouth, high-arched palate, low-set ears), cardiac and skeletal (hypoplastic thumbs and first metacarpals) abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402084011 Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type is a rare syndrome with cardiac malformations, characterised by prenatal-onset growth retardation (low birth weight and short stature), hypotonia, developmental delay and intellectual disability associated with microcephaly and craniofacial (low anterior hairline, hypotelorism, thick lips with carp-shaped mouth, high-arched palate, low-set ears), cardiac and skeletal (hypoplastic thumbs and first metacarpals) abnormalities. 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
Hadziselimovic syndrome Is a Microcephalus false Inferred relationship Some
Hadziselimovic syndrome Is a Congenital heart disease true Inferred relationship Some
Hadziselimovic syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Hadziselimovic syndrome Is a Congenital anomaly of brain false Inferred relationship Some
Hadziselimovic syndrome Is a Short stature disorder true Inferred relationship Some
Hadziselimovic syndrome Associated morphology Developmental anomaly false Inferred relationship Some 4
Hadziselimovic syndrome Occurrence Congenital true Inferred relationship Some 4
Hadziselimovic syndrome Finding site Heart structure false Inferred relationship Some 4
Hadziselimovic syndrome Occurrence Congenital false Inferred relationship Some 5
Hadziselimovic syndrome Associated morphology Developmental anomaly false Inferred relationship Some 6
Hadziselimovic syndrome Occurrence Congenital false Inferred relationship Some 6
Hadziselimovic syndrome Occurrence Congenital false Inferred relationship Some 7
Hadziselimovic syndrome Associated morphology Developmental anomaly false Inferred relationship Some 5
Hadziselimovic syndrome Finding site Limb structure false Inferred relationship Some 5
Hadziselimovic syndrome Finding site Face structure false Inferred relationship Some 6
Hadziselimovic syndrome Finding site Limb structure true Inferred relationship Some 4
Hadziselimovic syndrome Associated morphology Congenital smallness false Inferred relationship Some 7
Hadziselimovic syndrome Finding site Brain structure false Inferred relationship Some 7
Hadziselimovic syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Hadziselimovic syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Hadziselimovic syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Hadziselimovic syndrome Occurrence Congenital true Inferred relationship Some 3
Hadziselimovic syndrome Occurrence Congenital true Inferred relationship Some 2
Hadziselimovic syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Hadziselimovic syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Hadziselimovic syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Hadziselimovic syndrome Occurrence Congenital true Inferred relationship Some 1
Hadziselimovic syndrome Finding site Heart structure true Inferred relationship Some 2
Hadziselimovic syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
Hadziselimovic syndrome Finding site Face structure true Inferred relationship Some 1
Hadziselimovic syndrome Associated morphology Congenital smallness false Inferred relationship Some 3
Hadziselimovic syndrome Finding site Brain structure false Inferred relationship Some 3
Hadziselimovic syndrome Interprets Height / growth measure true Inferred relationship Some 5
Hadziselimovic syndrome Finding site Head structure true Inferred relationship Some 3
Hadziselimovic syndrome Is a Genetic disease true Inferred relationship Some
Hadziselimovic syndrome Has interpretation Below reference range true Inferred relationship Some 6
Hadziselimovic syndrome Interprets Birth head circumference true Inferred relationship Some 6
Hadziselimovic syndrome Is a Congenital microcephaly (disorder) true Inferred relationship Some
Hadziselimovic syndrome Has interpretation Below reference range true Inferred relationship Some 5
Hadziselimovic syndrome Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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