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72855002: Congenital prognathism (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
121005013 Congenital prognathism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
121007017 Prognathia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
121008010 Exognathia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
121009019 Progenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
121011011 Prognathism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
813178013 Congenital prognathism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1233550014 Big jaw en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
24101000077117 prognathisme congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital prognathism Is a Congenital anomaly of digestive system false Inferred relationship Some
Congenital prognathism Is a Congenital anomaly of jaw true Inferred relationship Some
Congenital prognathism Is a Dentofacial anomaly false Inferred relationship Some
Congenital prognathism Is a anomalie congénitale de l'appareil respiratoire false Inferred relationship Some
Congenital prognathism Finding site Bone structure of cranium false Inferred relationship Some 2
Congenital prognathism Finding site Cartilaginous tissue structure false Inferred relationship Some
Congenital prognathism Associated morphology Congenital forward deviation false Inferred relationship Some 1
Congenital prognathism Associated morphology Abnormally short growth (morphologic abnormality) false Inferred relationship Some 1
Congenital prognathism Occurrence Congenital false Inferred relationship Some
Congenital prognathism Finding site Jaw region structure false Inferred relationship Some 1
Congenital prognathism Associated morphology anomalie congénitale false Inferred relationship Some 2
Congenital prognathism Finding site Oral cavity structure false Inferred relationship Some
Congenital prognathism Finding site Tooth structure false Inferred relationship Some
Congenital prognathism Is a Congenital anomaly of skull false Inferred relationship Some
Congenital prognathism Is a Deformity (finding) false Inferred relationship Some
Congenital prognathism Associated morphology Congenital forward deviation false Inferred relationship Some 1
Congenital prognathism Associated morphology Abnormally short growth (morphologic abnormality) false Inferred relationship Some 1
Congenital prognathism Finding site Jaw region structure false Inferred relationship Some 1
Congenital prognathism Associated morphology anomalie congénitale false Inferred relationship Some 2
Congenital prognathism Finding site Bone structure of cranium false Inferred relationship Some 2
Congenital prognathism Occurrence Congenital false Inferred relationship Some 3
Congenital prognathism Associated morphology anomalie du développement false Inferred relationship Some 3
Congenital prognathism Is a Disorder of bone development (disorder) false Inferred relationship Some
Congenital prognathism Is a Disorder of skull (disorder) false Inferred relationship Some
Congenital prognathism Finding site Jaw region structure false Inferred relationship Some 3
Congenital prognathism Is a Oral deformity of jaw (disorder) false Inferred relationship Some
Congenital prognathism Occurrence Congenital false Inferred relationship Some 4
Congenital prognathism Associated morphology Congenital protrusion false Inferred relationship Some 4
Congenital prognathism Finding site Jaw region structure false Inferred relationship Some 4
Congenital prognathism Occurrence Congenital true Inferred relationship Some 1
Congenital prognathism Associated morphology Congenital deviation false Inferred relationship Some 1
Congenital prognathism Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital prognathism Finding site Bone structure of jaw (body structure) true Inferred relationship Some 1
Congenital prognathism Is a Congenital anomaly of face bones true Inferred relationship Some
Congenital prognathism Associated morphology Protrusion true Inferred relationship Some 1
Congenital prognathism Is a Congenital abnormality of skull and face bones false Inferred relationship Some
Congenital prognathism Is a Protrusion of bone true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Maxillary prognathism Is a False Congenital prognathism Inferred relationship Some
Mandibular prognathism Is a False Congenital prognathism Inferred relationship Some
Prognathism NOS Is a False Congenital prognathism Inferred relationship Some
The MMEP syndrome is a congenital syndromic form of split-hand/foot malformation. It is characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism. Intellectual deficit has been reported. MMEP syndrome is considered to be a very rare condition, although the exact prevalence remains unknown. The etiology is not completely understood. Disruption of the sorting nexin 3 gene (SNX3; 6q21) has been shown to play a causative role in MMEP, although this was not confirmed in recent studies. Is a True Congenital prognathism Inferred relationship Some
A rare, genetic, developmental defect during embryogenesis disorder characterized by abnormal forward projection of the mandible beyond the standard relation to the cranial base, with lower incisors often overlapping the upper incisors, that is inherited in an autosomal dominant manner. Association with mildly everted lower eyelids, flat malar area, thickened lower lip and craniosynostosis has been reported. Is a True Congenital prognathism Inferred relationship Some
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. Is a True Congenital prognathism Inferred relationship Some
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. Is a True Congenital prognathism Inferred relationship Some

This concept is not in any reference sets

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