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Cristae cutis
Dermal ridges
Dermatoglyphics
Epidermal
Epidermal pattern
Epidermal ridge
Epidermal ridge data
Epidermal ridges
Epidermic
Epidermical
Epidermous
Fingerprint
Fingerprint pattern
Fingerprint ridge
Friction ridge
Friction-ridge pattern
Papillary ridge
Pattern
Ridge
Ridge pattern
Ridge transform fault system
Ridge-pattern data
Ridge-transform fault system
Ridge-transform system
Skin ridges

Translation of "Epidermal ridge " (English → French) :

epidermal ridge data | ridge-pattern data

données lophoscopiques
IATE - European construction
IATE - European construction


epidermal ridge

crête épidermique
IATE - European construction | Migration
IATE - European construction | Migration


friction ridge | papillary ridge | epidermal ridge | fingerprint ridge | ridge

crête papillaire | crête dermique | ligne papillaire | crête dermatoglyphique | crête
médecine > médecine légale
médecine > médecine légale


cristae cutis | dermal ridges | skin ridges | epidermal ridges

crêtes papillaires | crêtes dermiques
médecine
médecine


A rare genetic developmental defect during embryogenesis disorder with characteristics of the lack of epidermal ridges on the palms and soles, resulting in the absence of fingerprints, with no other associated manifestations. It is associated with a

adermatoglyphie congénitale isolée
SNOMEDCT-BE (disorder) / 763748007
SNOMEDCT-BE (disorder) / 763748007


fingerprint pattern | pattern | dermatoglyphics | friction-ridge pattern | epidermal pattern | ridge pattern | fingerprint

dessin digital | dermatoglyphe | dessin papillaire | dessin épidermique | empreinte digitale
médecine > anatomie | médecine > médecine légale
médecine > anatomie | médecine > médecine légale


epidermal | epidermic | epidermical | epidermous

épidermique
IATE - Health
IATE - Health


ridge-transform system [ ridge/transform system | ridge-transform fault system | ridge/transform fault system | ridge transform fault system ]

système dorsale-faille transformante
Oceanography
Océanographie


A form of syndromic craniosynostosis with characteristics of craniosynostosis, mild facial dysmorphism (prominent supraorbital ridges, mild proptosis and maxillary hypoplasia) and calcification of the basal ganglia. The disease is associated with a f

syndrome de craniosynostose-calcifications intracrâniennes
SNOMEDCT-BE (prominent supraorbital ridges, mild proptosis and maxillary hypoplasia) and calcification of the basal ganglia. The disease is associated with a f / 720816004
SNOMEDCT-BE (disorder) / 720816004


A very rare hereditary skin disease with manifestation of irregularly distributed epidermal hyperkeratosis of the palms and soles. Reported in 35 families worldwide to date. The lesions usually start to develop in early adolescence but can also prese

kératodermie palmoplantaire ponctuée type 1
SNOMEDCT-BE (disorder) / 717184007
SNOMEDCT-BE (disorder) / 717184007




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'Epidermal ridge'

Date index:2023-02-10 -

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