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29696001: Prolapse (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
49677014 Prolapse en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49678016 Inferior displacement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49682019 Downward displacement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
760618016 Prolapse (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Prolapse Is a Displacement true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Cystocele - delivered with postpartum complication Associated morphology False Prolapse Inferred relationship Some 2
Vaginal enterocele (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Female rectocele and enterocele (disorder) Associated morphology True Prolapse Inferred relationship Some 2
Female rectocele and enterocele (disorder) Associated morphology True Prolapse Inferred relationship Some 3
Female rectocele and enterocele (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Acquired pelvic enterocele Associated morphology False Prolapse Inferred relationship Some 2
Acquired vaginal enterocele Associated morphology True Prolapse Inferred relationship Some 2
Acquired vaginal enterocele Associated morphology True Prolapse Inferred relationship Some 1
Congenital vaginal enterocele Associated morphology True Prolapse Inferred relationship Some 1
Congenital vaginal enterocele Associated morphology True Prolapse Inferred relationship Some 2
Prolapsed grade II internal hemorrhoid Associated morphology False Prolapse Inferred relationship Some 1
Prolapsed grade IV internal hemorrhoid Associated morphology False Prolapse Inferred relationship Some 2
Prolapsed grade III internal hemorrhoid Associated morphology False Prolapse Inferred relationship Some 2
A rare ophthalmic disorder characterized by bilateral ptosis, upper ocular movement limitation, absence of the lacrimal punctum and facial dysmorphism including, narrow and squared forehead, bilateral thick and arched eyebrows, absence of bilateral lower medial eyelashes, telecanthus, mild anteverted nostrils, a relatively long philtrum and maxillary hypoplasia. Some patients may have low set and dysplastic ears. Associated morphology True Prolapse Inferred relationship Some 2
Congenital dysgenetic ptosis Associated morphology True Prolapse Inferred relationship Some 1
Congenital prolapsed uterus Associated morphology True Prolapse Inferred relationship Some 1
Ptosis-vocal cord paralysis syndrome is a rare, hereditary disorder with ptosis characterized by the combination of congenital bilateral recurrent laryngeal nerve paralysis and congenital bilateral ptosis. There have been no further descriptions in the literature since 1983. Associated morphology True Prolapse Inferred relationship Some 3
Ptosis-vocal cord paralysis syndrome is a rare, hereditary disorder with ptosis characterized by the combination of congenital bilateral recurrent laryngeal nerve paralysis and congenital bilateral ptosis. There have been no further descriptions in the literature since 1983. Associated morphology True Prolapse Inferred relationship Some 4
Congenital prolapse of urinary bladder Associated morphology True Prolapse Inferred relationship Some 1
A rare syndrome characterized by the association of blepharophimosis and ptosis, V-esotropia, and weakness of extraocular and frontal muscles with syndactyly of the toes, short stature, prognathism, and hypertrophy and fusion of the eyebrows. Associated morphology True Prolapse Inferred relationship Some 3
A rare, genetic, lens position anomaly disease characterized by bilateral congenital blepharoptosis, ectopia lentis and high grade myopia. Additional reported manifestations include abnormally long eye globes and signs of levator aponeurosis disinsertion. There have been no further descriptions in the literature since 1982. Associated morphology True Prolapse Inferred relationship Some 1
Congenital ptosis of left upper eyelid (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Congenital prolapsed rectum Associated morphology True Prolapse Inferred relationship Some 1
Congenital Horner syndrome is a rare neurological disorder characterized by relative pupillary miosis and blepharoptosis, evident at birth, caused by interruption of the oculosympathetic innervation at any point along the neural pathway from the hypothalamus to the orbit. Often additional symptoms, such as enophthalmos, facial anhidrosis, iris heterochromia, conjunctival congestion, transient hypotonia and/or pupillary dilation lag, may be present. Association with birth trauma, neoplasms or vascular malformations has been reported. Associated morphology False Prolapse Inferred relationship Some 1
Congenital prolapse of urinary meatus (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Congenital ptosis of right upper eyelid (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Congenital prolapse of mucous membrane of urinary bladder Associated morphology True Prolapse Inferred relationship Some 1
Microbrachycephaly-ptosis-cleft lip syndrome is characterized by the association of intellectual deficit, microbrachycephaly, hypotelorism, palpebral ptosis, a thin/long face, cleft lip, and anomalies of the lumbar vertebra, sacrum and pelvis. It has been described in two Brazilian sisters. Transmission appears to be autosomal recessive. Associated morphology True Prolapse Inferred relationship Some 1
Congenital prolapse of aortic valve (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Congenital ptosis of bilateral upper eyelids (disorder) Associated morphology True Prolapse Inferred relationship Some 2
Congenital ptosis of bilateral upper eyelids (disorder) Associated morphology True Prolapse Inferred relationship Some 1
A rare disorder characterized by the association of ptosis, strabismus and ectopic pupils. It has been described in one family (in a mother and three of her children). Transmission is autosomal dominant. Associated morphology True Prolapse Inferred relationship Some 1
A rare syndrome characterized by congenital ptosis and posterior fusion of the lumbosacral vertebrae. It has been described in a mother and her two daughters. Associated morphology True Prolapse Inferred relationship Some 1
Laubry-Pezzi syndrome is a rare, non-syndromic, congenital heart malformation characterized by the prolapse of an aortic valve cusp into a subjacent ventricular septal defect due to Venturi effect, resulting in aortic regurgitation. Patients typically present with symptoms of progressive aortic valve insufficiency, such as shortness of breath, heart palpitations, chest pain and exercise intolerance. Associated morphology True Prolapse Inferred relationship Some 2
Laparoscopic ventral fixation of internal prolapse of rectum using mesh (procedure) Direct morphology True Prolapse Inferred relationship Some 1
Laparoscopic ventral fixation of internal prolapse of rectum using synthetic mesh (procedure) Direct morphology True Prolapse Inferred relationship Some 1
Laparoscopic ventral fixation of internal prolapse of rectum using biological mesh Direct morphology True Prolapse Inferred relationship Some 1
Ocular laceration with intraocular prolapse Associated morphology True Prolapse Inferred relationship Some 2
Vitreous prolapse of right eye (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Vitreous prolapse of left eye (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Arrhythmogenic bileaflet mitral prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Arrhythmogenic bileaflet mitral prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 2
Mitral valve posterior leaflet prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Ptosis of bilateral breasts (finding) Associated morphology True Prolapse Inferred relationship Some 2
Ptosis of bilateral breasts (finding) Associated morphology True Prolapse Inferred relationship Some 1
Combined anteroposterior colporrhaphy Direct morphology True Prolapse Inferred relationship Some 2
Posterior repair of vagina (procedure) Direct morphology True Prolapse Inferred relationship Some 1
Posterior repair of vagina with mesh (procedure) Direct morphology True Prolapse Inferred relationship Some 1
Colpoperineoplasty with repair of urethrocele Direct morphology True Prolapse Inferred relationship Some 1
Colpoperineoplasty with repair of urethrocele Direct morphology True Prolapse Inferred relationship Some 2
Plastic repair of urethrocele in female Direct morphology True Prolapse Inferred relationship Some 1
Plastic repair of urethrocele in female Direct morphology True Prolapse Inferred relationship Some 2
Colporrhaphy for repair of urethrocele Direct morphology True Prolapse Inferred relationship Some 1
Colporrhaphy for repair of urethrocele Direct morphology True Prolapse Inferred relationship Some 2
Vitreous prolapse of bilateral eyes (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Vitreous prolapse of bilateral eyes (disorder) Associated morphology True Prolapse Inferred relationship Some 2
Mechanical ptosis of left upper eyelid Associated morphology True Prolapse Inferred relationship Some 1
Mechanical ptosis of right upper eyelid (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Bilateral mechanical ptosis of upper eyelids Associated morphology True Prolapse Inferred relationship Some 1
Bilateral mechanical ptosis of upper eyelids Associated morphology True Prolapse Inferred relationship Some 2
Paralytic ptosis of left upper eyelid Associated morphology True Prolapse Inferred relationship Some 1
Paralytic ptosis of right upper eyelid (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Bilateral paralytic ptosis of upper eyelids Associated morphology True Prolapse Inferred relationship Some 1
Bilateral paralytic ptosis of upper eyelids Associated morphology True Prolapse Inferred relationship Some 2
Ptosis of right breast (finding) Associated morphology True Prolapse Inferred relationship Some 1
Ptosis of left breast (finding) Associated morphology True Prolapse Inferred relationship Some 1
Prolapse of right fallopian tube (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Prolapse of left fallopian tube Associated morphology True Prolapse Inferred relationship Some 1
Congenital prolapse of mitral valve Associated morphology True Prolapse Inferred relationship Some 1
Downward displacement of right half of diaphragm (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Downward displacement of left half of diaphragm (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Downward displacement of diaphragm Associated morphology True Prolapse Inferred relationship Some 1
Repair of ptosis of eyebrow Direct morphology True Prolapse Inferred relationship Some 1
Postoperative ptosis of eyelid Associated morphology True Prolapse Inferred relationship Some 2
Enterocele co-occurrent with complete uterovaginal prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Enterocele co-occurrent with complete uterovaginal prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 2
Enterocele co-occurrent with complete uterovaginal prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 3
Vaginal enterocele due to incomplete uterovaginal prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Vaginal enterocele due to incomplete uterovaginal prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 2
Female cystocele and uterine prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Female cystocele and uterine prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 2
Female cystocele and uterine prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 3
Cystocele with first degree uterine prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 3
Cystocele with second degree uterine prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 3
Cystocele with third degree uterine prolapse (disorder) Associated morphology True Prolapse Inferred relationship Some 3
A rare ophthalmic disorder characterized by blepharophimosis, ptosis, epicanthus inversus, and telecanthus, that can appear associated with (type 1) or without primary ovarian insufficiency (POI; type 2). Associated morphology True Prolapse Inferred relationship Some 2
A rare disorder of the ocular adnexa characterized by an extended phenotype of blepharophimosis, ptosis, epicanthus inversus and telecanthus syndrome (BPES). When BPES is caused by a microdeletion encompassing other genes in addition to the causative gene FOXL2, the patient has additional features including intellectual disability, external genital anomaly, spastic diplegia, and speech delay. Acquired microcephaly can also be observed. Associated morphology True Prolapse Inferred relationship Some 5
Prolapse of small intestine (disorder) Associated morphology True Prolapse Inferred relationship Some 1
A rare genetic multiple congenital anomalies/dysmorphic syndrome with variable intellectual disability characterized by abnormal head shape/metopic ridging and facial dysmorphism (which may include arched eyebrows, ptosis, downslanting palpebral fissures, epicanthal folds, and short upturned nose). Many patients present variable global developmental delay and/or autism spectrum disorder. Additional reported features are cardiac, skeletal, or urogenital anomalies. Brain imaging may show agenesis of the corpus callosum. Associated morphology True Prolapse Inferred relationship Some 1
Repair of blepharoptosis by levator muscle technique Direct morphology True Prolapse Inferred relationship Some 1
Repair of blepharoptosis by tarsolevator resection, internal approach Direct morphology True Prolapse Inferred relationship Some 2
Repair of blepharoptosis by tarsolevator resection, external approach Direct morphology True Prolapse Inferred relationship Some 2
Rectocele - delivered with postpartum complication Associated morphology False Prolapse Inferred relationship Some 2
Rectocele complicating postpartum care - baby delivered during previous episode of care Associated morphology False Prolapse Inferred relationship Some 2
Rectocele - baby delivered Associated morphology False Prolapse Inferred relationship Some 1
A rare syndromic disorder with strabismus with characteristics of congenital non-progressive ophthalmoplegia affecting the oculomotor and/or trochlear nucleus/nerve and their innervated muscles. Patients present with abnormal resting position of the eyes (in most cases infraducted and exotropic), limitation of vertical and horizontal gaze, impaired binocular vision, amblyopia, unilateral or bilateral blepharoptosis, and compensatory abnormal head posture. Extraocular manifestations include intellectual disability, peripheral neuropathy, and skeletal abnormalities among others. Associated morphology True Prolapse Inferred relationship Some 3
Vertical retraction syndrome Associated morphology True Prolapse Inferred relationship Some 2
Congenital fibrosis of inferior rectus muscle (disorder) Associated morphology True Prolapse Inferred relationship Some 2
Perianal plication of levator ani muscles and anal sphincters Direct morphology True Prolapse Inferred relationship Some 1
Ptosis of left eyelid following surgery (disorder) Associated morphology True Prolapse Inferred relationship Some 1
Ptosis of right eyelid following surgery Associated morphology True Prolapse Inferred relationship Some 1

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