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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
Emberger syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Hereditary lymphedema type I Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hereditary lymphedema type II Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hereditary lymphedema and yellow nails Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Cholestasis-edema syndrome, Norwegian type Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Distichiasis-lymphedema syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Male sexual precocity with adrenal hyperplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Psychosocial short stature Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Male pseudohermaphroditism due to congenital adrenal hyperplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Female pseudohermaphroditism due to congenital adrenal hyperplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Pseudohermaphroditism due to congenital adrenal hyperplasia 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 2
Hyperostosis cranialis interna Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Hyperostosis cranialis interna Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Progressive scapulohumeroperoneal distal myopathy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Virilization of female due to adrenal hyperfunction Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Primary lymphedema with systemic and visceral involvement Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Primary lymphedema with systemic involvement Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Primary lymphedema with visceral involvement Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Primary lymphedema due to syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Phospholipase A2 activating protein-associated neurodevelopmental disorder Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Severe myopia, generalized joint laxity, short stature syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Severe myopia, generalized joint laxity, short stature syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Diaphragmatic hernia, short bowel, asplenia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Diaphragmatic hernia, short bowel, asplenia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Diaphragmatic hernia, short bowel, asplenia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 4
Diaphragmatic hernia, short bowel, asplenia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 8
Hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, xerostomia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital fibrosis syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital fibrosis syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Vertical retraction syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Vertical retraction syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital fibrosis of inferior rectus muscle Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Congenital fibrosis of inferior rectus muscle Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital kyphoscoliosis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome, hydroxylysine-deficient Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Ehlers-Danlos syndrome kyphoscoliotic and deafness type Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 7
Ehlers-Danlos syndrome kyphoscoliotic type Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 5
Microcephalus with brachydactyly and kyphoscoliosis syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 7
Congenital membrane of lacrimal punctum Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital corneal leukoma Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital distortion of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital expansion of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital colobomatous cyst of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital colobomatous cyst of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital absence of eye with orbital implant Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Fetal encasement syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital combined bony and soft tissue deformity of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital combined bony and soft tissue deformity of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital complete absence of nasolacrimal drainage system Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital contraction of orbit Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Keppen Lubinsky syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Pierpont syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Microcephalic primordial dwarfism, insulin resistance syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 3
Congenital anomaly of retina of left eye Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital anomaly of retina of right eye Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital abnormality of left lacrimal drainage system Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital abnormality of right lacrimal drainage system Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital abnormality of bilateral lacrimal drainage systems Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital abnormality of bilateral lacrimal drainage systems Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Congenital malformation of blood vessel of left orbit proper Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital malformation of blood vessel of right orbit proper Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital malformation of blood vessel of bilateral orbits proper Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Paraspadias Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Perineal hypospadias Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Prune exopolyphosphatase 1-related neurological syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Ring finger protein 13-related severe early-onset epileptic encephalopathy Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Pancreatic agenesis, holoprosencephaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Pancreatic agenesis, holoprosencephaly syndrome Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Early-onset calcifying leukoencephalopathy, skeletal dysplasia Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Single umbilical cord artery type II Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Single umbilical cord artery type I Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Single umbilical cord artery type III Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Single umbilical cord artery type IV Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 2
Ephrin receptor B4-related lymphatic-related hydrops fetalis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Cadherin EGF LAG seven-pass G-type receptor 1-related late-onset primary lymphedema Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Congenital primary lymphedema of Gordon Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1
Gap junction protein gamma 2-related late-onset primary lymphedema Pathological process True Pathological developmental process Inferred relationship Existential restriction modifier 1

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