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276752006: Embryological remnant (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
413034011 Embryological remnant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
669705010 Embryological remnant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
130431000077115 reliquat embryonnaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

135 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryological remnant Is a Congenital disease false Inferred relationship Some
Embryological remnant Occurrence Congenital false Inferred relationship Some
Embryological remnant Is a Congenital malformation true Inferred relationship Some
Embryological remnant Is a trouble selon la localisation corporelle false Inferred relationship Some
Embryological remnant Occurrence Congenital true Inferred relationship Some 1
Embryological remnant Associated morphology Persistent embryonic structure true Inferred relationship Some 1
Embryological remnant Finding site Embryonic structure false Inferred relationship Some 1
Embryological remnant Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Band of Ladd Is a True Embryological remnant Inferred relationship Some
Simonart's band Is a True Embryological remnant Inferred relationship Some
Persistent Gartner's duct Is a True Embryological remnant Inferred relationship Some
Mullerian remnant Is a True Embryological remnant Inferred relationship Some
Vestigial gastrointestinal remnant Is a True Embryological remnant Inferred relationship Some
Cervical thymic remnant Is a True Embryological remnant Inferred relationship Some
An abnormality involving one or more ovaries, occurring in women who have had a hysterectomy without bilateral oophorectomy. Is a False Embryological remnant Inferred relationship Some
Persisting fifth aortic arch Is a False Embryological remnant Inferred relationship Some
Common truncus arteriosus (disorder) Is a False Embryological remnant Inferred relationship Some
Persistent primary vitreous Is a False Embryological remnant Inferred relationship Some
Persistence of primitive artery Is a True Embryological remnant Inferred relationship Some
Epoophoron Is a True Embryological remnant Inferred relationship Some
Persistent cloaca (disorder) Is a True Embryological remnant Inferred relationship Some
Patent urachus (disorder) Is a True Embryological remnant Inferred relationship Some
Persistent lanugo Is a True Embryological remnant Inferred relationship Some
Persistent left posterior cardinal vein Is a False Embryological remnant Inferred relationship Some
Persistent dorsal mesentery Is a True Embryological remnant Inferred relationship Some
Persistent tunica vasculosa lentis Is a True Embryological remnant Inferred relationship Some
Persistent tuberculum impar Is a True Embryological remnant Inferred relationship Some
Persistent urogenital sinus Is a True Embryological remnant Inferred relationship Some
Patent vitelline duct (disorder) Is a False Embryological remnant Inferred relationship Some
Persistent thyroglossal duct Is a True Embryological remnant Inferred relationship Some
A rare congenital anomaly of the inferior vena cava characterized by the postnatal presence of a eustachian valve remnant, which may be asymptomatic and considered a normal variant or prominent and clinically significant. Clinical presentation is variable and includes obstruction of the inferior vena cava, cyanosis, thrombosis, pulmonary embolism, infective endocarditis, and when combined with persistent foramen ovale, it may generate permanent right-to-left shunt. Is a True Embryological remnant Inferred relationship Some
Vitellointestinal band Is a False Embryological remnant Inferred relationship Some
Paroophoron Is a True Embryological remnant Inferred relationship Some
Venous remnant Is a True Embryological remnant Inferred relationship Some
Ecchordosis physaliphora Is a True Embryological remnant Inferred relationship Some
Intra-abdominal vitelline remnant Is a False Embryological remnant Inferred relationship Some
Congenital anomaly of first branchial cleft (disorder) Is a False Embryological remnant Inferred relationship Some
Infection of urachal remnant (disorder) Is a True Embryological remnant Inferred relationship Some
Urachal sinus (disorder) Is a True Embryological remnant Inferred relationship Some
A rare otorhinolaryngological malformation characterized by the presence of a cyst, sinus or fistula occurring along the anterior border of the sternocleidomastoid muscle. Second branchial cleft fistulae and sinuses present with skin opening with chronic discharge and recurrent infections, whereas second branchial cleft cysts present as a painless, nontender, stable in size or slowly enlarging lateral neck masses. Cysts occasionally acutely increase in size during upper respiratory tract infection, leading to respiratory compromise, torticollis, and dysphagia. Is a False Embryological remnant Inferred relationship Some
A rare otorhinolaryngeal malformation characterized by a soft, fluctuant mass, abscess or draining tract along the anterior border of the lower half of sternocleidomastoid muscle, occasionally leading to development of retropharyngeal abscess, acute suppurative thyroiditis, stridor, respiratory distress, odynophagia and dysphagia. Anomaly occurs as a tract from the piriform sinus to the thyroid gland. A third branchial cleft fistula passes superficial to both the superior and recurrent laryngeal nerves, which is the main difference in comparison to the fourth branchial cleft fistula. Is a False Embryological remnant Inferred relationship Some
A rare otorhinolaryngeal malformation characterized by a soft, fluctuant mass, abscess or draining tract along the anterior border of the lower half of sternocleidomastoid muscle, occasionally leading to development of retropharyngeal abscess, acute suppurative thyroiditis, stridor, respiratory distress, odynophagia, and dysphagia. Anomaly occurs as a tract from the piriform sinus to the thyroid gland. A fourth branchial cleft fistula passes deep to the superior laryngeal nerve but superficial to the recurrent laryngeal nerve, which is the main difference in comparison to the third branchial cleft fistula. Is a False Embryological remnant Inferred relationship Some
Congenital prepapillary vascular loop Is a True Embryological remnant Inferred relationship Some
Persistent hyperplastic primary vitreous Is a True Embryological remnant Inferred relationship Some
Naso-palatine duct cyst Is a True Embryological remnant Inferred relationship Some
Vestigial remnants of canal of Cloquet Is a True Embryological remnant Inferred relationship Some
Persistent left superior vena cava Is a True Embryological remnant Inferred relationship Some
Nodular renal blastema Is a True Embryological remnant Inferred relationship Some
Persistent human tail Is a True Embryological remnant Inferred relationship Some
Arterial embryological remnant (disorder) Is a True Embryological remnant Inferred relationship Some
Developmental anomaly of vitelline duct (disorder) Is a True Embryological remnant Inferred relationship Some
Preauricular fistula Is a True Embryological remnant Inferred relationship Some
Patent foramen ovale Is a True Embryological remnant Inferred relationship Some
Persistent pupillary membranes Is a True Embryological remnant Inferred relationship Some
Branchial cleft anomaly Is a True Embryological remnant Inferred relationship Some
Myelinated nerve fibers of optic disc Is a True Embryological remnant Inferred relationship Some
Myelinated nerve fiber layer of retina Is a True Embryological remnant Inferred relationship Some
A rare closed dysraphism with terminal stalk with characteristics of persistant rudimentary spinal cord below conus. It contains non-functional neural tissue and is typically isolated. The diagnostic is suggested by attenuated conus without fat, further confirmed by pathological analysis (glioneuronal core with ependyma-lined lumen, nerve roots, and dorsal root ganglia). Differential diagnostic with intraoperative neurophysiological monitoring is mandatory as neuroimaging fails to distinguish it from functional conus. Is a True Embryological remnant Inferred relationship Some

This concept is not in any reference sets

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