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57697001: Growth alteration (morphologic abnormality)

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
95947010 Growth alteration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character 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
64911000077113 modification de la croissance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2499 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Growth alteration Is a Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Disturbance of hair cycle Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Loose anagen hair syndrome Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Gingival fibromatosis and hypertrichosis syndrome Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Telogen effluvium of the newborn (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic telogen effluvium (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Acute telogen effluvium (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
à l'examen : hirsutisme Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrichosis of lower eyelid Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare form of localized hypertrichosis characterized by hair growth near the laryngeal prominence during childhood. Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Trichiasis (disorder) Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Telogen hair loss caused by drug Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrichosis with congenital macrogingivae (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Anagen effluvium caused by drug Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 3
Congenital hypertrichosis (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Syndrom des akromegaloiden Gesichtes mit Hypertrichose Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypotrichosis following infectious disease (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypertrichosis lanuginosa (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Rombo syndrome Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Bilateral trichiasis Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrichia Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 1
Hirsutism (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrichosis cubiti (disorder) Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital negative ulnar variant of wrist Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital positive ulnar variant of wrist Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Abnormally short growth Is a True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept)
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 Existential restriction modifier (core metadata concept) 1
Congenital incomplete expansion Is a True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept)
Congenital redundant rectal mucosa Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital overexpansion Is a True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept)
Congenital smallness Is a False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept)
Failure of growth of fetal left cardiac ventricle Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Failure of growth of fetal right cardiac ventricle Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Reduction of gigantism of foot Direct morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital abnormal number Is a False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept)
Congenital growth disproportion Is a True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept)
Abnormally short and broad growth (morphologic abnormality) Is a False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept)
Abnormally long growth (morphologic abnormality) Is a True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept)
Infantile spasm and broad thumb syndrome (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Microdontia (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Single tooth microdontia Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Localized microdontia Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Relative generalized microdontia (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Paired teeth microdontia Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, hypoplastic type with microdontia Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
True generalised microdontia Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertaurodontism Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Single tooth macrodontia (disorder) Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Macrodontia Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Localised macrodontia Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypotrichosis of bilateral eyelids Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypotrichosis of bilateral eyelids Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypotrichosis and deafness syndrome (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital deafness with labyrinthine aplasia, microtia and microdontia Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 5
Relative generalized macrodontia Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare form of localized hypertrichosis characterized by hair growth near the laryngeal prominence during childhood. Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 2
Syndrom des akromegaloiden Gesichtes mit Hypertrichose Associated morphology False Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract-hypertrichosis-intellectual disability syndrome is characterised by congenital cataract, generalised 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 Existential restriction modifier (core metadata concept) 1
Hypertrichosis cubiti (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Wiedemann Steiner syndrome (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hallermann-Streiff syndrome (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 3
An extremely rare type of severe combined immunodeficiency syndrome (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 Existential restriction modifier (core metadata concept) 3
Barber-Say syndrome Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 5
Congenital generalized hypertrichosis (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal growth abnormality (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Twins with discordant fetal growth (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Maxillary jaw size anomaly Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Macrogenia Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Vertical maxillary excess Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypotrichosis of right upper eyelid (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypotrichosis of left upper eyelid Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypotrichosis of left eyelid (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypotrichosis of right eyelid Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked congenital generalized hypertrichosis Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal microcephaly (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic fetal brain disruption sequence Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypotrichosis of right lower eyelid (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypotrichosis of left lower eyelid (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 6
Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 3
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypertrichosis caused by drug (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hirsutism caused by drug (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Toxic anagen effluvium Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 8
Hypertrichosis of bilateral eyelids Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrichosis of right eyelid (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrichosis of left eyelid Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital ulnar positive variant of left wrist Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital ulnar positive variant of right wrist (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital positive ulnar variant of bilateral wrists Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital positive ulnar variant of bilateral wrists Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypertrichosis of right lower eyelid Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrichosis of right upper eyelid (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrichosis of left lower eyelid (disorder) Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrichosis of left upper eyelid Associated morphology True Growth alteration Inferred relationship Existential restriction modifier (core metadata concept) 1

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