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Anomaly
Congenital anomaly
Deformity
Diagnosis and management of hereditary disorders
Disease or lesion
Geothermal anomaly
Hereditary anomaly
Hereditary disposition
Hereditary leukocytic hypersegmentation
Hereditary predisposition
Hyposegmentation
Latent
Leukomelanopathy
May-Hegglin
Medical genetics
Multiple anomalies
NOS of brain
Pelger-Huët
Prepsychotic
Prodromal
Pseudoneurotic
Pseudopsychopathic
Schizotypal personality disorder
Temperature anomaly
Thermal anomaly

Traduction de «Hereditary anomaly » (Anglais → Néerlandais) :



Nail-patella syndrome is a rare hereditary patellar dysostosis with characteristics of nail hypoplasia or aplasia, aplastic or hypoplastic patellae, elbow dysplasia, and the presence of iliac horns as well as renal and ocular anomalies.

nagel-patella-syndroom


Anomaly (granulation)(granulocyte) or syndrome:Alder | May-Hegglin | Pelger-Huët | Hereditary:leukocytic:hypersegmentation | hyposegmentation | leukomelanopathy

anomalie (granulatie)(granulocyt) of syndroom van | Alder | anomalie (granulatie)(granulocyt) of syndroom van | May-Hegglin | anomalie (granulatie)(granulocyt) of syndroom van | Pelger-Huët | hereditaire | leukocytaire | hypersegmentatie | hereditaire | leukocytaire | hyposegmentatie | hereditaire | leukomelanopathie


An inherited, mild, non-hemolytic subtype of hereditary stomatocytosis that is associated with a temperature-dependent anomaly in red cell membrane permeability to potassium that leads to high in vitro potassium levels in samples stored below 37°C. N

familiale pseudohyperkaliëmie


geothermal anomaly | temperature anomaly | thermal anomaly

geothermische anomalie | temperatuuranomalie | thermische anomalie | warmte-anomalie


hereditary disposition | hereditary predisposition

erfelijke aanleg


X-linked mental retardation with characteristics of Brain anomalies, severe mental Retardation, Ectodermal dysplasia, Skeletal deformities (vertebral anomalies, scoliosis, polydactyly), Ear/eye anomalies (maldevelopment, small optic nerves, low set a

syndroom van malformatie van hersenen, ernstige verstandelijke beperking, ectodermale dysplasie, deformiteit van skelet, malformatie van oor en/of oog en dysplasie van nier


diagnosis and management of hereditary disorders | medical genetics

medische genetica


Congenital:anomaly | deformity | disease or lesion | multiple anomalies | NOS of brain

congenitale | anomalie | NNO van hersenen | congenitale | misvorming | NNO van hersenen | congenitale | multipele anomalieën | NNO van hersenen | congenitale | ziekte of laesie | NNO van hersenen |


Definition: A disorder characterized by eccentric behaviour and anomalies of thinking and affect which resemble those seen in schizophrenia, though no definite and characteristic schizophrenic anomalies occur at any stage. The symptoms may include a cold or inappropriate affect; anhedonia; odd or eccentric behaviour; a tendency to social withdrawal; paranoid or bizarre ideas not amounting to true delusions; obsessive ruminations; thought disorder and perceptual disturbances; occasional transient quasi-psychotic episodes with intense illusions, auditory or other ...[+++]

Omschrijving: Een stoornis die wordt gekenmerkt door excentriek gedrag en afwijkingen van denken en affect gelijkend op die welke bij schizofrenie worden gezien, hoewel er in geen enkel stadium zekere en kenmerkende schizofrene afwijkingen optreden. De symptomen kunnen omvatten: een ingeperkt of niet passend affect; anhedonie; zonderling of excentriek gedrag; een neiging tot sociale teruggetrokkenheid; paranoïde of bizarre ideeën die niet tot echte wanen worden; obsessief rumineren; stoornissen in het denken en in de waarneming; nu en dan optredende passagère quasi psychotische episoden met intense illusies, akoestische of andersoortige hallucinaties en waanachtige ideeën, do ...[+++]




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Date index: 2022-01-12
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