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248290002: Developmental delay (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
111041000077119 retard de développement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
370667011 Developmental delay en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
382731000077112 retard de développement (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
638573019 Developmental delay (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

130 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
retard de développement Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
retard de développement est un(e) (attribut) trouble du développement true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Cyclin-dependent kinase-like 5 deficiency (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
dysplasie spondylo-épimétaphysaire type Geneviève est un(e) (attribut) True retard de développement Inferred relationship Some
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
syndrome de cataracte congénitale-surdité-retard de développement sévère est un(e) (attribut) True retard de développement Inferred relationship Some
Pancytopenia with developmental delay syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
Lethal polymalformative syndrome Boissel type est un(e) (attribut) True retard de développement Inferred relationship Some
Xp22.13p22.2 duplication syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder) est un(e) (attribut) False retard de développement Inferred relationship Some
retard dans le développement sexuel et/ou de la puberté est un(e) (attribut) True retard de développement Inferred relationship Some
Phonological delay est un(e) (attribut) True retard de développement Inferred relationship Some
retard de langage est un(e) (attribut) True retard de développement Inferred relationship Some
retard de langage expressif est un(e) (attribut) True retard de développement Inferred relationship Some
Receptive language delay est un(e) (attribut) True retard de développement Inferred relationship Some
Delayed pre-verbal development est un(e) (attribut) True retard de développement Inferred relationship Some
Clumsiness - motor delay est un(e) (attribut) True retard de développement Inferred relationship Some
Gross motor development delay (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
PPM-X syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
Developmental delay in receptive-expressive language (disorder) est un(e) (attribut) False retard de développement Inferred relationship Some
Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Cutis laxa-corneal clouding-oligophrenia syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
syndrome de microdélétion 16p11.2 proximale est un(e) (attribut) True retard de développement Inferred relationship Some
Distal 16p11.2 microdeletion syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
Beta-D-mannosidosis est un(e) (attribut) True retard de développement Inferred relationship Some
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Spastic paraplegia, severe developmental delay, epilepsy syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
SATB2-associated syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
Joint contractures, developmental delay, Pierre Robin syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
1p35.2 microdeletion syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
9q33.3q34.11 microdeletion syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
16p13.2 microdeletion syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Xq25 microduplication syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
17q24.2 microdeletion syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
11q22.2q22.3 microdeletion syndrome est un(e) (attribut) True retard de développement Inferred relationship Some
8q24.3 microdeletion syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Limb girdle muscular dystrophy due to POMK deficiency est un(e) (attribut) True retard de développement Inferred relationship Some
Cognitive developmental delay (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Developmental delay in feeding (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Global developmental delay est un(e) (attribut) True retard de développement Inferred relationship Some
Development delay NOS est un(e) (attribut) False retard de développement Inferred relationship Some
Developmental delay in fine motor function (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Developmental delay in social skills est un(e) (attribut) True retard de développement Inferred relationship Some
Family history of neurological developmental delay constatation associée (attribut) True retard de développement Inferred relationship Some 1
Koolen De Vries syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Cardiocranial syndrome Pfeiffer type (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Bohring Opitz syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Frank-Ter Haar syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some
syndrome d'obésité, colite, hypothyroïdie, hypertrophie cardiaque, retard de développement est un(e) (attribut) True retard de développement Inferred relationship Some
Trigonocephaly, short stature, developmental delay syndrome (disorder) est un(e) (attribut) True retard de développement Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Description inactivation indicator reference set

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