FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.9.0  |  FHIR Version n/a  User: [n/a]

308490002: Pathological developmental process (qualifier value)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
451847013 Pathological developmental process en Synonym Active Entire term case insensitive SNOMED CT core module
705033019 Pathological developmental process (qualifier value) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pathological developmental process Is a Pathological process true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
WT limb blood syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Keratoderma hereditarium mutilans with ichthyosis syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lack of ossification of vomer Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
CK syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Lack of ossification of mandible Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital hypoplastic anemia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lymphedema hypoparathyroidism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Lack of ossification of premaxilla Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Multiple lentigines syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lack of ossification of pubis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Revesz syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 6
Cervical spinal hydromeningocele Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 2
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 4
Congenital vaginal enterocele Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital vaginal enterocele Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Craniosynostosis and dental anomalies syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Craniosynostosis and dental anomalies syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Xylosyltransferase 1 congenital disorder of glycosylation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Autosomal recessive frontotemporal pachygyria Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Mandibular hypoplasia, deafness, progeroid syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Intellectual disability, facial dysmorphism, hand anomalies syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Intellectual disability, facial dysmorphism, hand anomalies syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Roifman syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Roifman syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lack of ossification of supraoccipital bone Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Delayed epiphyseal closure Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Discontinuity between mitral valve and pulmonary valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Quadricuspid pulmonary valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital abnormality of arterial valves Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Premature epiphyseal closure Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Lack of ossification of tympanic anulus Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Right-left orientation of bicuspid pulmonary valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Bone turnover rate disorder Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Bone turnover rate decreased Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Congenital fusion of pulmonary valve segment Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 2
Increased bone formation Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Anterior-posterior orientation of bicuspid pulmonary valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Oligodontia and cancer predisposition syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Oligodontia and cancer predisposition syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Poikiloderma, alopecia, retrognathism, cleft palate syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Bicuspid pulmonary valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Unicuspid aortic valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Commissural fusion of pulmonary valve Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 2
Bone resorption disorder Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 1
Sacral agenesis Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 2
Sacral agenesis Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
9q31.1q31.3 microdeletion syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Split hand, split foot malformation with sensorineural hearing loss syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Split hand, split foot malformation with sensorineural hearing loss syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Lack of ossification of basisphenoid bone Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Decreased maintenance of bone matrix Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Acommissural unicuspid aortic valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Bone turnover rate increased Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Lack of ossification of lacrimal bone Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Epiphysis closure disorder Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital abnormality of cardiac ventricle Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Bone turnover rate absent Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Commissural fusion of aortic valve Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 2
Late closure of anterior fontanel Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Progression of fetal right ventricular outflow tract obstruction Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 2
Incomplete ossification of ilium Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Decreased osteoblast function Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Progression of fetal left ventricular outflow tract obstruction Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 2
Accessory tissue on pulmonary valve cusp Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Incomplete ossification of interparietal bone Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Lack of bone formation Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Lack of ossification of premaxilla Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Quadricuspid aortic valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Unicommissural unicuspid aortic valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Osteoid formation disorder Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 1
Lack of ossification of presphenoid bone Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Epiphysis formation disorder Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 1
Early fontanel closure Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Congenital hypoplasia of ulna and split foot syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Functional bone disorder Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 1
Reduced ossification Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 2
Incomplete ossification of bone Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Late fontanel closure Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Short ulna, dysmorphism, hypotonia, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Short ulna, dysmorphism, hypotonia, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
13q12.3 microdeletion syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
14q24.1q24.3 microdeletion syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Mandibulofacial dysostosis, macroblepharon, macrostomia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Mandibulofacial dysostosis, macroblepharon, macrostomia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Epidermolysis bullosa simplex due to exophilin 5 deficiency Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to BP230 deficiency Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hypoplastic left heart syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Spondylocostal dysostosis, hypospadias, intellectual disability syndrome Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3

Start Previous Page 98 of 149 Next End

This concept is not in any reference sets

Back to Start