FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  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
Cornual placenta accreta Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Aprosencephaly/atelencephaly spectrum Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Aprosencephaly Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
XK aprosencephaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Aprosencephaly cerebellar dysgenesis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Aprosencephaly cerebellar dysgenesis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Aprosencephaly cerebellar dysgenesis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Aprosencephaly cerebellar dysgenesis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Morbidly adherent placenta Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Placenta increta Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Cornual placenta accreta Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Adherent placenta Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Extensive peripapillary myelinated nerve fibers of retina Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Myelinated nerve fiber layer of retina Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Regressive spondylometaphyseal dysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
nudE neurodevelopment protein 1-related microhydranencephaly Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
nudE neurodevelopment protein 1-related microhydranencephaly Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Cerebellar-facial-dental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Cerebellar-facial-dental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Cerebellar-facial-dental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Cerebellar-facial-dental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Short stature, developmental delay, congenital heart defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Osteosclerotic metaphyseal dysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Osteosclerotic metaphyseal dysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Symptomatic form of Coffin-Lowry syndrome in female carrier Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Fatty acyl-coenzyme A reductase 1 deficiency Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Congenital insensitivity to pain with severe intellectual disability Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 7
16p12.1p12.3 triplication syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
16p12.1p12.3 triplication syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
4q25 proximal deletion syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
4q25 proximal deletion syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Lamb Shaffer syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
12p12.1 microdeletion syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Atrial septal defect within oval fossa Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital infiltrating lipomatosis of face Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital infiltrating lipomatosis of face Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
X-linked intellectual disability, hypotonia, movement disorder syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Generalized inflammatory peeling skin syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Generalized non-inflammatory peeling skin syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital prepapillary vascular loop Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital prepapillary vascular loop Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 3 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Waardenburg syndrome type 3 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Waardenburg syndrome type 1 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Myopathic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Myopathic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Myopathic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Myopathic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Classical-like Ehlers-Danlos syndrome type 2 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Classical-like Ehlers-Danlos syndrome type 2 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Classical-like Ehlers-Danlos syndrome type 2 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Ichthyosis hystrix gravior Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Mirror-image polydactyly Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Oculocerebrodental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Oculocerebrodental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Oculocerebrodental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Oculocerebrodental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Oculocerebrodental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Congenital myopathy with reduced type 2 muscle fibers Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
X-linked myotubular myopathy, abnormal genitalia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
X-linked myotubular myopathy, abnormal genitalia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Spastic ataxia, dysarthria due to glutaminase deficiency Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Hypopigmentation-immunodeficiency disease type 1 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hypopigmentation-immunodeficiency disease type 1 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Hypopigmentation-immunodeficiency disease type 3 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hypopigmentation-immunodeficiency disease type 3 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
X-linked intellectual disability, short stature, overweight syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital umbilical hernia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Localized junctional epidermolysis bullosa non-Herlitz type Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital isolated onychodysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1

Start Previous Page 147 of 149 Next End

This concept is not in any reference sets

Back to Start