57697001: Growth alteration (morphologic abnormality)

SNOMED CT Concept\Body structure (body structure)\Morphologically altered structure\Morphologically abnormal structure\Growth alteration

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

95947010 Growth alteration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

95950013 Disturbance of growth en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

796347018 Growth alteration (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

64911000077113 modification de la croissance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Growth alteration	Is a	Morphologically abnormal structure	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hypertrichosis of left upper eyelid (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
A lethal form of pontocerebellar hypoplasia with characteristics of prenatal onset of microcephaly, hypoplasia of the cerebellum, brainstem, and spinal cord, dysmorphic craniofacial features such as sloping forehead and micrognathia, and multiple contractures. Supratentorial atrophy has also been reported.	Associated morphology	True	Growth alteration	Inferred relationship	Some	6
Abnormal number (morphologic abnormality)	Is a	True	Growth alteration	Inferred relationship	Some
Abnormal smallness (morphologic abnormality)	Is a	True	Growth alteration	Inferred relationship	Some
Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome.	Associated morphology	True	Growth alteration	Inferred relationship	Some	3
A rare disorder related to monochorionic twin pregnancy with characteristics of unequal placental sharing leading to growth restriction in one twin according to the following criteria: estimated fetal weight (EFW) of one twin below the 3rd percentile as a solitary parameter, or fulfilment of at least two out of four contributory parameters (EFW of one twin below the 10th percentile, abdominal circumference of one twin below the 10th percentile, EFW discordance of ≥ 25%, umbilical artery pulsatility index of the smaller twin above the 95th percentile). Early severe forms are associated with a significant risk of intrauterine demise or neurological adverse outcome for both twins.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterised by variable intellectual disability and/or developmental delay, epilepsy, generalised hypertrichosis, severe gingival overgrowth and visual impairment in some patients. Common craniofacial features include bitemporal narrowing, bushy and straight eyebrows, long eyelashes, low-set ears, deep/short philtrum, everted upper lip, prominent upper and lower vermilion, wide mouth, micrognathia, and retrognathia.	Associated morphology	True	Growth alteration	Inferred relationship	Some	3
Abnormally broad growth (morphologic abnormality)	Is a	True	Growth alteration	Inferred relationship	Some
Schöpf-Schulz-Passarge syndrome	Associated morphology	True	Growth alteration	Inferred relationship	Some	6
Congenital asymmetry of kidneys (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1

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