FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

720430002: Acrofacial dysostosis Rodriguez type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3320731017 Acrofacial dysostosis Rodriguez type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3320732012 Acrofacial dysostosis Rodriguez type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5402331019 A rare, severe, multiple congenital anomalies syndrome characterized by severe mandibular hypoplasia, upper limb phocomelia with oligodactyly, absent fibula, and a number of additional skeletal (hypoplastic scapula and ischii, 11 ribs, clubfeet), facial (hypertelorism, hypoplastic supraorbital ridges, wide nasal bridge, microtia with low-set ears) and variable internal organ abnormalities (including arhinencephaly, hypolobulated lungs, and congenital cardiac defects), which usually lead to perinatal death. Surviving patients show features similar to Nagel syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402332014 A rare, severe, multiple congenital anomalies syndrome characterised by severe mandibular hypoplasia, upper limb phocomelia with oligodactyly, absent fibula, and a number of additional skeletal (hypoplastic scapula and ischii, 11 ribs, clubfeet), facial (hypertelorism, hypoplastic supraorbital ridges, wide nasal bridge, microtia with low-set ears) and variable internal organ abnormalities (including arhinencephaly, hypolobulated lungs, and congenital cardiac defects), which usually lead to perinatal death. Surviving patients show features similar to Nagel syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acrofacial dysostosis Rodriguez type (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Is a Congenital anomaly of face bones true Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Is a Longitudinal deficiency of limb true Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Is a Dysostosis true Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Occurrence Congenital true Inferred relationship Some 3
Acrofacial dysostosis Rodriguez type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 4
Acrofacial dysostosis Rodriguez type (disorder) Occurrence Congenital false Inferred relationship Some 4
Acrofacial dysostosis Rodriguez type (disorder) Finding site Bone structure of face false Inferred relationship Some 4
Acrofacial dysostosis Rodriguez type (disorder) Occurrence Congenital false Inferred relationship Some 5
Acrofacial dysostosis Rodriguez type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 3
Acrofacial dysostosis Rodriguez type (disorder) Finding site Bone structure of extremity true Inferred relationship Some 3
Acrofacial dysostosis Rodriguez type (disorder) Associated morphology Abnormal shortening false Inferred relationship Some 5
Acrofacial dysostosis Rodriguez type (disorder) Finding site Entire limb false Inferred relationship Some 5
Acrofacial dysostosis Rodriguez type (disorder) Is a Lesion of face true Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Occurrence Congenital true Inferred relationship Some 1
Acrofacial dysostosis Rodriguez type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Acrofacial dysostosis Rodriguez type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Acrofacial dysostosis Rodriguez type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Acrofacial dysostosis Rodriguez type (disorder) Occurrence Congenital true Inferred relationship Some 2
Acrofacial dysostosis Rodriguez type (disorder) Finding site Entire limb true Inferred relationship Some 1
Acrofacial dysostosis Rodriguez type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Acrofacial dysostosis Rodriguez type (disorder) Associated morphology Abnormal shortening true Inferred relationship Some 1
Acrofacial dysostosis Rodriguez type (disorder) Finding site Bone structure of face true Inferred relationship Some 2
Acrofacial dysostosis Rodriguez type (disorder) Is a Congenital deformity false Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Associated morphology Dysplasia true Inferred relationship Some 3
Acrofacial dysostosis Rodriguez type (disorder) Associated morphology Dysplasia true Inferred relationship Some 2
Acrofacial dysostosis Rodriguez type (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Acrofacial dysostosis Rodriguez type (disorder) Is a Congenital dysplasia of limb (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start