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719140001: X-gebonden syndroom van verstandelijke beperking, dysmorfie en cerebrale atrofie (aandoening)


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
3315146015 X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3315147012 X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3315148019 Prieto Badia Mulas syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6956871000146116 syndroom van Prieto-Badia-Mulas nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6956881000146119 X-gebonden syndroom van mentale retardatie, dysmorfie en cerebrale atrofie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7495761000146117 X-gebonden syndroom van verstandelijke beperking, dysmorfie en cerebrale atrofie (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7719321000146115 X-gebonden syndroom van verstandelijke beperking, dysmorfie en cerebrale atrofie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7869011000146112 X-gebonden syndroom van verstandelijke handicap, dysmorfie en cerebrale atrofie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3315149010 This syndrome has characteristics of intellectual deficit associated with facial dysmorphism, patella luxation and abnormal growth of the teeth. It has been described in eight males from multiple generations of one family. The locus for the causative gene for this syndrome has been located to the region between p11.22 and p21.1 on the X chromosome. 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
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a mentale retardatie false Inferred relationship Some
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a X-linked hereditary disease false Inferred relationship Some
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a Cerebral atrophy true Inferred relationship Some
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a Hereditary disorder of nervous system false Inferred relationship Some
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 5
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Occurrence Congenital false Inferred relationship Some 5
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Associated morphology Atrophy false Inferred relationship Some 4
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Finding site Cerebrum false Inferred relationship Some 4
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Finding site Limb structure true Inferred relationship Some 3
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Finding site Face structure false Inferred relationship Some 5
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a Intellectual disability true Inferred relationship Some
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Finding site Face structure true Inferred relationship Some 1
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Finding site Cerebrum true Inferred relationship Some 2
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Associated morphology Atrophy true Inferred relationship Some 2
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a X-linked recessive hereditary disease true Inferred relationship Some
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 4
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 4
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 5
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 5
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Is a Congenital neurological disorder (disorder) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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