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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
Laryngeal cleft type 0 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Macular dystrophy of substantia propria of cornea of bilateral eyes Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Macular dystrophy of substantia propria of cornea of bilateral eyes Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital cyst of nasolacrimal duct Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Exstrophy epispadias complex Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital deformity of upper limb Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Megaconial congenital muscular dystrophy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Megaconial congenital muscular dystrophy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Microphthalmia, microtia, fetal akinesia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Microphthalmia, microtia, fetal akinesia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Microphthalmia, microtia, fetal akinesia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Microphthalmia, microtia, fetal akinesia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Microphthalmia, microtia, fetal akinesia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Congenital deformity of hand Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of bilateral upper limbs Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of bilateral upper limbs Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital anomaly of right upper limb Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of left upper limb Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Contactin associated protein 2-related developmental and epileptic encephalopathy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital deformity of shoulder Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital deformity of upper arm Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Common arterial trunk with crossed over pulmonary arteries Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Isolated hypoplasia of fovea centralis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Primary failure of tooth eruption Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of second branchial cleft Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of second branchial cleft Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital anomaly of third branchial cleft Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of third branchial cleft Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital anomaly of fourth branchial cleft Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of fourth branchial cleft Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital fistula of commissure of lips Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Non-syndromic metopic craniosynostosis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Non-syndromic metopic craniosynostosis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Isolated osteopoikilosis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
46,XY disorder of sex development due to isolated 17,20-lyase deficiency Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Autosomal dominant generalized dystrophic epidermolysis bullosa Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of left lower limb Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of right lower limb Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Situs ambiguus Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Cardiac anomaly and heterotaxy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Polysplenia heterotaxy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Ebstein's anomaly of left sided tricuspid valve with discordant atrioventricular connections Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital malformation of blood vessel of bilateral orbits proper Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Incomplete cleft lip Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Meningoencephalocele of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Meningoencephalocele of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Meningoencephalocele of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Meningoencephalocele of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Complete cleft lip Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital meningocele of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Syndromic nanophthalmos due to Kenny-Caffey syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital meningocele of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Isolated agenesis of cerebellar vermis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Placenta fenestrata Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Cyst of fetal Rathke pouch Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Rathke's pouch cyst Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Osteofibrous dysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
46,XX ovotesticular disorder of sex development Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Ovotesticular disorder of sex development Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital azygos continuation of inferior vena cava Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital straddling and overriding tricuspid valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital cochleovestibular malformation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital vascular malformation of orbital region Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Persistent congenital anteversion of femur Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Encephalopathy due to mitochondrial and peroxisomal fission defect Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Phosphodiesterase 4D haploinsufficiency syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Phosphodiesterase 4D haploinsufficiency syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital atrioventricular septal defect Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of atrioventricular septum Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
FG syndrome type 1 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
FG syndrome type 1 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Dermatosparaxis Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Dermatosparaxis Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Dermatosparaxis Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Embryopathy caused by isotretinoin Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Night blindness, skeletal anomalies, dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Night blindness, skeletal anomalies, dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital abnormal retraction of nipple Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Otodental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Symptomatic form of fragile X syndrome in female carrier Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Symptomatic form of fragile X syndrome in female carrier Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
46,XX ovarian dysgenesis, short stature syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Caroli syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Placenta accreta Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Placenta percreta Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Cornual placenta accreta Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4

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