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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
Peg-shaped tooth Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Bilobate placenta Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Trisomy 13, meiotic nondisjunction Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Trisomy 13 - mitotic nondisjunction mosaicism Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Trisomy 13 - mitotic nondisjunction mosaicism Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Trisomy 18 - mitotic nondisjunction mosaicism Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Nonfenestrated interatrial communication within oval fossa Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Palmoplantar hyperkeratosis sclerodactyly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Palmoplantar hyperkeratosis sclerodactyly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Fetal mediastinal shift to right Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Fetal mediastinal shift to left Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
X-linked oligodontia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Camptodactyly of finger Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital absence of one tooth Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Split spinal cord malformation type I Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Split spinal cord malformation type I Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Split spinal cord malformation type I Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome, hydroxylysine-deficient Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Ehlers-Danlos syndrome kyphoscoliotic type Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Mayer Rokitansky Küster Hauser syndrome type 1 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Mayer Rokitansky Küster Hauser syndrome type 1 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Mayer Rokitansky Küster Hauser syndrome type 1 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Proximal interphalangeal joint symphalangism Cushing type Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
XK aprosencephaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Malformation of teeth Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Epiphyseal arrest due to and following traumatic injury Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital accessory tissue of tricuspid valve Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hydrocephalus with anomaly of aqueduct of Sylvius Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Chondrodysplasia punctata, X-linked dominant type Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
N syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Generalized peeling skin syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Hereditary skin peeling syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Acral peeling skin syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Non syndromic dextrocardia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Non syndromic camptodactyly of fingers Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Gemination of tooth Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Foreign accent syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Agenesis of cervical vertebra Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital deformity of bone of forearm Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hemimaxillofacial dysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 6
Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Tall stature, intellectual disability, renal anomalies syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Overgrowth syndrome with 2q37 translocation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Overgrowth syndrome with 2q37 translocation Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Low density lipoprotein receptor-related protein 5 related primary osteoporosis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Craniofrontonasal dysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Deafness-dystonia-optic neuronopathy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Ocular anomalies, axonal neuropathy, developmental delay syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Early-onset epilepsy, intellectual disability, brain anomalies syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
TBC1 domain containing kinase-related intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
SIX homeobox 2-related frontonasal dysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
SIX homeobox 2-related frontonasal dysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Camptodactyly syndrome Guadalajara type 3 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Camptodactyly syndrome Guadalajara type 3 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Camptodactyly syndrome Guadalajara type 3 Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Split-foot malformation, mesoaxial polydactyly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Split-foot malformation, mesoaxial polydactyly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Split-foot malformation, mesoaxial polydactyly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Thickened dental follicle Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Fried syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Incontinentia pigmenti syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Incontinentia pigmenti syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Incontinentia pigmenti syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Prenatal-onset spinal muscular atrophy with congenital bone fractures Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Prenatal-onset spinal muscular atrophy with congenital bone fractures Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Disorder of fetus caused by propylthiouracil Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Adenylosuccinate synthetase-like 1-related distal myopathy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1

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