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308490002: Pathological developmental process (qualifier value)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
451847013 Pathological developmental process en Synonym Active Case insensitive SNOMED CT core
705033019 Pathological developmental process (qualifier value) en Fully specified name Active Case insensitive SNOMED CT core


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
Placenta fenestrata Pathological process True Pathological developmental process Inferred relationship Some 2
Cyst of craniobuccal pouch Pathological process True Pathological developmental process Inferred relationship Some 1
Rathke's pouch cyst Pathological process True Pathological developmental process Inferred relationship Some 1
Limb girdle muscular dystrophy due to POMK deficiency Pathological process True Pathological developmental process Inferred relationship Some 1
Osteofibrous dysplasia Pathological process True Pathological developmental process Inferred relationship Some 2
MIRAGE syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
MIRAGE syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
46,XX ovotesticular disorder of sex development Pathological process True Pathological developmental process Inferred relationship Some 1
Ovotesticular disorder of sex development Pathological process True Pathological developmental process Inferred relationship Some 1
Congenital azygos continuation of inferior vena cava Pathological process True Pathological developmental process Inferred relationship Some 1
Congenital straddling and overriding tricuspid valve Pathological process True Pathological developmental process Inferred relationship Some 1
Congenital cochleovestibular malformation Pathological process True Pathological developmental process Inferred relationship Some 1
Congenital vascular malformation of orbital region Pathological process True Pathological developmental process Inferred relationship Some 1
Persistent congenital anteversion of femur Pathological process True Pathological developmental process Inferred relationship Some 1
Encephalopathy due to mitochondrial and peroxisomal fission defect Pathological process True Pathological developmental process Inferred relationship Some 3
PDE4D haploinsufficiency syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
PDE4D haploinsufficiency syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
DONSON-related microcephaly, short stature, limb abnormalities spectrum Pathological process True Pathological developmental process Inferred relationship Some 1
DONSON-related microcephaly, short stature, limb abnormalities spectrum Pathological process True Pathological developmental process Inferred relationship Some 2
Congenital atrioventricular septal defect Pathological process True Pathological developmental process Inferred relationship Some 1
Congenital anomaly of atrioventricular septum Pathological process True Pathological developmental process Inferred relationship Some 1
FG syndrome type 1 Pathological process True Pathological developmental process Inferred relationship Some 1
FG syndrome type 1 Pathological process True Pathological developmental process Inferred relationship Some 2
Dermatosparaxis Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Dermatosparaxis Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Dermatosparaxis Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
Isotretinoin syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Night blindness, skeletal anomalies, dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Night blindness, skeletal anomalies, dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Congenital abnormal retraction of nipple Pathological process True Pathological developmental process Inferred relationship Some 1
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
Otodental syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Symptomatic form of fragile X syndrome in female carrier Pathological process True Pathological developmental process Inferred relationship Some 1
Symptomatic form of fragile X syndrome in female carrier Pathological process True Pathological developmental process Inferred relationship Some 2
46,XX ovarian dysgenesis, short stature syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Caroli syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Hydrops, lactic acidosis, sideroblastic anaemia, multisystemic failure syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Placenta accreta Pathological process True Pathological developmental process Inferred relationship Some 2
Placenta percreta Pathological process True Pathological developmental process Inferred relationship Some 2
Cornual placenta accreta Pathological process True Pathological developmental process Inferred relationship Some 4
Aprosencephaly/atelencephaly spectrum Pathological process True Pathological developmental process Inferred relationship Some 1
Aprosencephaly Pathological process True Pathological developmental process Inferred relationship Some 2
XK aprosencephaly syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Aprosencephaly cerebellar dysgenesis Pathological process True Pathological developmental process Inferred relationship Some 1
Aprosencephaly cerebellar dysgenesis Pathological process True Pathological developmental process Inferred relationship Some 2
Aprosencephaly cerebellar dysgenesis Pathological process True Pathological developmental process Inferred relationship Some 3
Aprosencephaly cerebellar dysgenesis Pathological process True Pathological developmental process Inferred relationship Some 4
Morbidly adherent placenta Pathological process True Pathological developmental process Inferred relationship Some 3
Placenta increta Pathological process True Pathological developmental process Inferred relationship Some 3
Cornual placenta accreta Pathological process True Pathological developmental process Inferred relationship Some 2
Adherent placenta Pathological process True Pathological developmental process Inferred relationship Some 2
Extensive peripapillary myelinated nerve fibres of retina Pathological process True Pathological developmental process Inferred relationship Some 1
Myelinated nerve fibre layer of retina Pathological process True Pathological developmental process Inferred relationship Some 1
Regressive spondylometaphyseal dysplasia Pathological process True Pathological developmental process Inferred relationship Some 1
CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation Pathological process True Pathological developmental process Inferred relationship Some 3
Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
PYCR2-related microcephaly, progressive leucoencephalopathy Pathological process True Pathological developmental process Inferred relationship Some 1
NDE1-related microhydranencephaly Pathological process True Pathological developmental process Inferred relationship Some 1
NDE1-related microhydranencephaly Pathological process True Pathological developmental process Inferred relationship Some 2
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Some 4
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Pathological process True Pathological developmental process Inferred relationship Some 5
Cerebellar-facial-dental syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Cerebellar-facial-dental syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Cerebellar-facial-dental syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
Cerebellar-facial-dental syndrome Pathological process True Pathological developmental process Inferred relationship Some 4
Short stature, developmental delay, congenital heart defect syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Osteosclerotic metaphyseal dysplasia Pathological process True Pathological developmental process Inferred relationship Some 1
Osteosclerotic metaphyseal dysplasia Pathological process True Pathological developmental process Inferred relationship Some 3
Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome Pathological process True Pathological developmental process Inferred relationship Some 4
Symptomatic form of Coffin-Lowry syndrome in female carrier Pathological process True Pathological developmental process Inferred relationship Some 1
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
Fatty acyl-CoA reductase 1 deficiency Pathological process True Pathological developmental process Inferred relationship Some 5
Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency Pathological process True Pathological developmental process Inferred relationship Some 5
Congenital insensitivity to pain with severe intellectual disability Pathological process True Pathological developmental process Inferred relationship Some 7
16p12.1p12.3 triplication syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
16p12.1p12.3 triplication syndrome Pathological process True Pathological developmental process Inferred relationship Some 4
MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
4q25 proximal deletion syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
4q25 proximal deletion syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
Lamb Shaffer syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
12p12.1 microdeletion syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
Spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
Spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
Spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Some 3
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Some 1
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Some 2
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Pathological process True Pathological developmental process Inferred relationship Some 4
Ostium secundum type atrial septal defect Pathological process True Pathological developmental process Inferred relationship Some 1
Congenital infiltrating lipomatosis of face Pathological process True Pathological developmental process Inferred relationship Some 1
Congenital infiltrating lipomatosis of face Pathological process True Pathological developmental process Inferred relationship Some 2
Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome Pathological process True Pathological developmental process Inferred relationship Some 1

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Reference Sets

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