FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

308490002: Pathological developmental process (qualifier value)

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

Descriptions:

Id Description Lang Type Status Case? Module
451847013 Pathological developmental process en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
705033019 Pathological developmental process (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
213321000052110 patologisk utvecklingsprocess sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pathological developmental process Is a Pathological process true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Rupture of congenital aneurysm of cerebral artery (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Severe myoclonic epilepsy in infancy Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Early myoclonic encephalopathy Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Multiple mitochondrial dysfunctions syndrome type 2 (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Multiple congenital anomalies, hypotonia, seizures syndrome type 2 Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
FAST kinase domains 2-related infantile mitochondrial encephalomyopathy (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Rasmussen syndrome Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Febrile infection related epilepsy syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 3
Combined oxidative phosphorylation defect type 27 Pathological process (attribute) True Pathological developmental process Inferred relationship Some 3
Congenital velopharyngeal incompetence Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 3
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 4
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 5
Congenital hypoplasia of testis and scrotum (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Congenital occlusion of ureteral orifice (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome Pathological process (attribute) True Pathological developmental process Inferred relationship Some 3
Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome Pathological process (attribute) True Pathological developmental process Inferred relationship Some 4
Right streak ovary (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Left streak ovary (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Hypothalamic hamartoma with gelastic seizure Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Fanconi anemia of complementation group C Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Isolated aplasia of optic nerve (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Triopia Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Triopia Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Triopia Pathological process (attribute) True Pathological developmental process Inferred relationship Some 3
Triopia Pathological process (attribute) True Pathological developmental process Inferred relationship Some 4
Inverse Klippel Trénaunay syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Inverse Klippel Trénaunay syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Inverse Klippel Trénaunay syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 3
Congenital dysplasia of limb (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Congenital malformation of right renal vein (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Congenital malformation of left renal vein (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Congenital malformation of renal vein Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Congenital anomaly of left renal vein (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Congenital anomaly of right renal vein (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Congenital anomaly of renal vein (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Congenital bowing of long bone (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 3
Ehlers-Danlos syndrome classic type 2 Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Ehlers-Danlos syndrome classic type 2 Pathological process (attribute) True Pathological developmental process Inferred relationship Some 2
Ehlers-Danlos syndrome classic type 2 Pathological process (attribute) True Pathological developmental process Inferred relationship Some 3
Short stature for age due to Turner syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Delayed puberty in male due to hypogonadotropic hypogonadism (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Short stature for age due to Noonan syndrome (disorder) Pathological process (attribute) True Pathological developmental process Inferred relationship Some 1
Neuropsychiatric disorder Pathological process (attribute) True Pathological developmental process Inferred relationship Some 3

Start Previous Page 150 of 150

This concept is not in any reference sets

Back to Start