FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.6  |  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
Congenital cystic dilatation of common bile duct Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Central basal perimembranous ventricular septal defect Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Macrodactyly of finger of left hand Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Macrodactyly of finger of right hand Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital shortening of left Achilles tendon Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital shortening of right Achilles tendon Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lymphedema, posterior choanal atresia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Dysraphism, cleft lip and palate, limb reduction defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Dysraphism, cleft lip and palate, limb reduction defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Dysraphism, cleft lip and palate, limb reduction defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Dysraphism, cleft lip and palate, limb reduction defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Dysraphism, cleft lip and palate, limb reduction defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Severe oculo-renal-cerebellar syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Eye defects, arachnodactyly, cardiopathy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Eye defects, arachnodactyly, cardiopathy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Eye defects, arachnodactyly, cardiopathy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Fryns Smeets Thiry syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital hydrocephalus, low insertion of umbilicus syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital hydrocephalus, low insertion of umbilicus syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital hydrocephalus, low insertion of umbilicus syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Microcephalic osteodysplastic primordial dwarfism type II Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Microcephalic osteodysplastic primordial dwarfism type II Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Autosomal recessive congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Autosomal dominant congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Autosomal dominant congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Placenta accreta without hemorrhage Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Placenta accreta Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 3
Epibulbar lipodermoid, preauricular appendage, polythelia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Epibulbar lipodermoid, preauricular appendage, polythelia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Epibulbar lipodermoid, preauricular appendage, polythelia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Epibulbar lipodermoid, preauricular appendage, polythelia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Progressive cerebello-cerebral atrophy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Distal arthrogryposis type 10 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Special AT-rich sequence-binding protein 2-associated syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Special AT-rich sequence-binding protein 2-associated syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Autosomal dominant deafness with onychodystrophy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Autosomal dominant deafness with onychodystrophy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Autosomal dominant deafness with onychodystrophy syndrome Pathological process False Pathological developmental process Inferred relationship Existential restriction modifier 5
Short umbilical cord Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital abnormal fusion of right carpal bones Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital dysplasia of bilateral upper limbs Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital dysplasia of bilateral upper limbs Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital dysplasia of right upper limb Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital abnormal fusion of bilateral carpal bones Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital abnormal fusion of bilateral carpal bones Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital dysplasia of left upper limb Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital abnormal fusion of left carpal bones Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Congenital kyphosis of cervicothoracic spine Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
4H leukodystrophy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Polymicrogyria due to tubulin beta 2B class IIb mutation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 6
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Congenital anomaly of craniovertebral junction Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital kyphosis of cervicothoracic spine Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Joint contractures, developmental delay, Pierre Robin syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Joint contractures, developmental delay, Pierre Robin syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Cerebral ventriculomegaly, cystic kidney disease Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Mandibulofacial dysostosis with alopecia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Incomplete achromatopsia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Primary lymphedema Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lymphedema praecox Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Primary lymphedema tardum Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hereditary lymphedema Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital elevation of bilateral scapulae Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital absence of left lower leg and foot Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital absence of left lower leg and foot Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital absence of right lower leg and foot Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital absence of right lower leg and foot Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lymphedema, posterior choanal atresia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Lymphedema hypoparathyroidism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
German syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Emberger syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2

Start Previous Page 143 of 149 Next End

This concept is not in any reference sets

Back to Start