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
Disturbance of hair cycle	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Loose anagen hair syndrome	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
A rare autosomal dominant disorder characterized by a generalized enlargement of the gingiva occurring at birth or during childhood that is associated with generalized hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback.	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
Telogen effluvium of the newborn (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Chronic telogen effluvium (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
Acute telogen effluvium (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
à l'examen : hirsutisme	Associated morphology	False	Growth alteration	Inferred relationship	Some	1
Hypertrichosis of lower eyelid	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
A rare form of localized hypertrichosis characterized by hair growth near the laryngeal prominence during childhood.	Associated morphology	False	Growth alteration	Inferred relationship	Some	2
Trichiasis (disorder)	Associated morphology	False	Growth alteration	Inferred relationship	Some	2
Telogen hair loss caused by drug	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypertrichosis with congenital macrogingivae (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Anagen effluvium caused by drug (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
A rare, syndromic, inherited retinal disorder characterized by cone-rod type congenital amaurosis, severe retinal dystrophy leading to visual impairment and profound photophobia (without night blindness), and trichomegaly (bushy eyebrows with synophrys, excessive facial and body hair including marked circumareolar hypertrichosis). There have been no further descriptions in the literature since 1989.	Associated morphology	False	Growth alteration	Inferred relationship	Some	3
A rare genetic syndrome characterized by the association of congenital hypertrichosis in the anterior cervical region with peripheral sensory and motor neuropathy. Associated features may include retinal anomalies, spina bifida, kyphoscoliosis and hallux valgus, and developmental delay (one case). There have been no further descriptions in the literature since 1993.	Associated morphology	False	Growth alteration	Inferred relationship	Some	3
Congenital hypertrichosis	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
syndrome d'hypertrichose-faciès acromégaloïde	Associated morphology	False	Growth alteration	Inferred relationship	Some	3
Hypotrichosis following infectious disease (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
Congenital hypertrichosis lanuginosa (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Rombo syndrome is characterized by vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, peripheral vasodilation with cyanosis and basal cell carcinomas.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Bilateral trichiasis	Associated morphology	False	Growth alteration	Inferred relationship	Some	1
Atrichia	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hirsutism (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypertrichosis cubiti is a rare hair anomaly characterized by symmetrical, congenital or early-onset, bilateral hypertrichosis localized on the extensor surfaces of the upper extremities (especially the elbows). Short stature, or other abnormalities, such as developmental delay, facial anomalies and intellectual disability, may or may not be associated.	Associated morphology	False	Growth alteration	Inferred relationship	Some	4
Congenital negative ulnar variant of wrist (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Condition where the ulna projects more distally relative to the radius.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Abnormally short growth (morphologic abnormality)	Is a	True	Growth alteration	Inferred relationship	Some
A rare cutaneous paraneoplastic disease characterised by the presence of excessive lanugo-type hair on the glabrous skin of face, neck, trunk and limbs that can be associated with additional clinical features such as burning glossitis, papillary hypertrophy of the tongue, diarrhoea, dysgeusia, and/or weight loss. It is associated with lymphoma or cancer of the gastrointestinal system, urinary tract, lung, breast, uterus or ovary.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Congenital incomplete expansion	Is a	True	Growth alteration	Inferred relationship	Some
Congenital redundant rectal mucosa	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Congenital overexpansion	Is a	True	Growth alteration	Inferred relationship	Some
Congenital smallness	Is a	False	Growth alteration	Inferred relationship	Some
Failure of growth of fetal left cardiac ventricle	Associated morphology	False	Growth alteration	Inferred relationship	Some	1
Failure of growth of fetal right cardiac ventricle	Associated morphology	False	Growth alteration	Inferred relationship	Some	1
Reduction of gigantism of foot	Direct morphology	False	Growth alteration	Inferred relationship	Some	1
Congenital abnormal number	Is a	False	Growth alteration	Inferred relationship	Some
Congenital growth disproportion	Is a	True	Growth alteration	Inferred relationship	Some
Abnormally short and broad growth	Is a	False	Growth alteration	Inferred relationship	Some
Abnormally long growth (morphologic abnormality)	Is a	True	Growth alteration	Inferred relationship	Some
Infantile spasms-broad thumbs syndrome is a rare neurologic disorder characterized by profound developmental delay, facial dysmorphism (i.e. microcephaly, large anterior fontanel, hypertelorism, downslanting palpebral fissures, beaked nose, micrognathia), broad thumbs and flexion and/or extension spasms. Bilateral cataracts, hypertrophic cardiomyopathy and hydrocele have also been reported. EEG shows hypsarrhythmic features and MRI may reveal partial agenesis of the corpus callosum, mild brain atrophy and/or ventriculomegaly. There have been no further descriptions in the literature since 1990.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Microdontia	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Single tooth microdontia	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Localized microdontia	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Relative generalised microdontia	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Paired teeth microdontia (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Amelogenesis imperfecta, hypoplastic type with microdontia	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
True generalized microdontia	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypertaurodontism	Associated morphology	False	Growth alteration	Inferred relationship	Some	2
Single tooth macrodontia (disorder)	Associated morphology	False	Growth alteration	Inferred relationship	Some	1
Macrodontia	Associated morphology	False	Growth alteration	Inferred relationship	Some	1
Localized macrodontia	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypotrichosis of bilateral eyelids	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypotrichosis of bilateral eyelids	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
A syndromic genetic deafness characterized by erythrokeratoderma, hypotrichosis, nail dystrophy and sensorineural hearing loss. Erythema, recurrent skin infections and mucositis have also been associated.	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome.	Associated morphology	False	Growth alteration	Inferred relationship	Some	5
Relative generalised macrodontia	Associated morphology	False	Growth alteration	Inferred relationship	Some	2
A rare form of localized hypertrichosis characterized by hair growth near the laryngeal prominence during childhood.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
A rare genetic syndrome characterized by the association of congenital hypertrichosis in the anterior cervical region with peripheral sensory and motor neuropathy. Associated features may include retinal anomalies, spina bifida, kyphoscoliosis and hallux valgus, and developmental delay (one case). There have been no further descriptions in the literature since 1993.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
A rare, syndromic, inherited retinal disorder characterized by cone-rod type congenital amaurosis, severe retinal dystrophy leading to visual impairment and profound photophobia (without night blindness), and trichomegaly (bushy eyebrows with synophrys, excessive facial and body hair including marked circumareolar hypertrichosis). There have been no further descriptions in the literature since 1989.	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
syndrome d'hypertrichose-faciès acromégaloïde	Associated morphology	False	Growth alteration	Inferred relationship	Some	1
Cataract-hypertrichosis-intellectual disability syndrome is characterized by congenital cataract, generalized hypertrichosis and intellectual deficit. It has been described in two Egyptian siblings born to consanguineous parents. It is transmitted as an autosomal recessive trait.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypertrichosis cubiti is a rare hair anomaly characterized by symmetrical, congenital or early-onset, bilateral hypertrichosis localized on the extensor surfaces of the upper extremities (especially the elbows). Short stature, or other abnormalities, such as developmental delay, facial anomalies and intellectual disability, may or may not be associated.	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
A rare, genetic multiple congenital anomalies/dysmorphic syndrome characterized by short stature, hypertrichosis (most commonly of the back or elbow regions), facial dysmorphism, behavioral problems, developmental delay and, most commonly, mild to moderate intellectual disability.	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hallermann-Streiff syndrome	Associated morphology	True	Growth alteration	Inferred relationship	Some	3
An extremely rare type of severe combined immunodeficiency (SCID) characterized by the classical signs of T-B- SCID (severe and recurrent infections, diarrhea, failure to thrive, absence of T and B lymphocytes), associated with skeletal anomalies like short stature, bowing of the long bones and metaphyseal abnormalities of variable degree of severity.	Associated morphology	False	Growth alteration	Inferred relationship	Some	3
Barber-Say syndrome (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	5
Congenital generalized hypertrichosis (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Fetal growth abnormality	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Twins with discordant fetal growth (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
Maxillary jaw size anomaly	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Macrogenia	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Vertical maxillary excess	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypotrichosis of right upper eyelid (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypotrichosis of left upper eyelid	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypotrichosis of left eyelid (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypotrichosis of right eyelid	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
X-linked congenital generalized hypertrichosis	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Fetal microcephaly (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Sporadic fetal brain disruption sequence is a rare, non-syndromic, central nervous system malformation disorder characterized by severe microcephaly (average occipitofrontal circumference -5.8 SD), overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly.	Associated morphology	True	Growth alteration	Inferred relationship	Some	3
A rare genetic syndrome with limb malformations as a major feature characterized by preaxial polydactyly of the hands and feet with variable phenotypic expressivity in combination with hypertrichosis extending from the posterior hairline to the middle of the back. Reported limb malformations include triphalangeal thumbs, duplicated thumbs, preaxial extra ray, and syndactyly between digits I and II in the hands, and large or duplicated hallux and syndactyly between toes I and II in the feet.	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
Hypotrichosis of right lower eyelid	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypotrichosis of left lower eyelid (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by the association of severe intellectual disability, strabismus, and anterior maxillary protrusion with vertical maxillary excess, open bite, and prominent crowded teeth. Mild cochlear hearing loss has been reported in addition.	Associated morphology	True	Growth alteration	Inferred relationship	Some	6
A rare, genetic, neurodevelopmental disorder characterized by global developmental delay, congenital heart defects, generalized hypertrichosis and dysmorphic facial features, most commonly triangular face, thick arched eyebrows, widely spaced eyes, posteriorly rotated low set ears, depressed nasal bridge, broad nasal root and tip, and pointed chin.	Associated morphology	True	Growth alteration	Inferred relationship	Some	3
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome is a rare, genetic developmental defect during embryogenesis malformation syndrome characterized by intrauterine growth restriction, flexion arthrogryposis of all joints, severe microcephaly, renal cystic dysplasia/agenesis/hypoplasia and complex malformations of the brain (cerebral and cerebellar hypoplasia, vermis, corpus callosum and/or occipital lobe agenesis, with or without arhinencephaly), as well as of the genitourinary tract (ureteral agenesis/hypoplasia, uterine hypoplasia and/or vaginal atresia), leading to fetal demise.	Associated morphology	True	Growth alteration	Inferred relationship	Some	3
Hypertrichosis caused by drug (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hirsutism caused by drug (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Toxic anagen effluvium	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
A rare ectodermal dysplasia syndrome characterized by hypotrichosis, tooth enamel hypoplasia, hypoplastic nails, palmoplantar keratoderma, hyperhidrosis on hands, face, and scalp, bilateral partial cutaneous syndactyly, and dysmorphic facial features with large prominent ear pinnae, pointed nose, and thin upper lips. Association of cardiomegaly has also been reported.	Associated morphology	True	Growth alteration	Inferred relationship	Some	8
Hypertrichosis of bilateral eyelids	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypertrichosis of right eyelid (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypertrichosis of left eyelid	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Congenital ulnar positive variant of left wrist (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Congenital ulnar positive variant of right wrist (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Congenital positive ulnar variant of bilateral wrists	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Congenital positive ulnar variant of bilateral wrists	Associated morphology	True	Growth alteration	Inferred relationship	Some	2
Hypertrichosis of right lower eyelid (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypertrichosis of right upper eyelid (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypertrichosis of left lower eyelid (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1
Hypertrichosis of left upper eyelid (disorder)	Associated morphology	True	Growth alteration	Inferred relationship	Some	1

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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