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Constitutional
Crop type
Dialing type
Dialling type
EC whole-vehicle type-approval
ECWVTA
EU whole-vehicle type-approval
EUWVTA
Forest crop type
Forest site type
Forest stand type
Forest type
Haemoglobinuria
Haemolytic anaemia cold type
Laron-like syndrome
Laron-type
Morquio
Pan-European type-approval
Psychosocial
Sanfilippo
Short stature NOS
Stand type
Touch type
Type at speed
Type of dialing
Type of dialling
Type quickly
Typing at speed
Vehicle type approval
WVTA
Warm type
Whole-vehicle type-approval

Translation of "Laron-type " (English → French) :

Short stature:NOS | constitutional | Laron-type | psychosocial

Insuffisance staturale:SAI | constitutionnelle | de type Laron | psychosociale


Laron-like syndrome

syndrome de Laron avec déficit immunitaire


crop type | forest crop type | forest site type | forest stand type | forest type | stand type

type forestier


EC whole-vehicle type-approval | ECWVTA | EU whole-vehicle type-approval | pan-European type-approval | vehicle type approval | whole-vehicle type-approval | EUWVTA [Abbr.] | WVTA [Abbr.]

réception par type de véhicule


touch type | type quickly | type at speed | typing at speed

taper vite


dialing type | dialling type | type of dialing | type of dialling

type de numérotation


Autoimmune haemolytic disease (cold type)(warm type) Chronic cold haemagglutinin disease Cold agglutinin:disease | haemoglobinuria | Haemolytic anaemia:cold type (secondary)(symptomatic) | warm type (secondary)(symptomatic)

Anémie hémolytique:type chaud (secondaire) (symptomatique) | type froid (secondaire) (symptomatique) | Hémoglobinurie à agglutinines froides Maladie (à):agglutinines froides | chronique à hémagglutinines froides | hémolytique auto-immune (type chaud) (type froid)


A group of tyrosine related oculocutaneous albinism (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i

albinisme oculo-cutané type 1


Beta-glucuronidase deficiency Mucopolysaccharidosis, types III, IV, VI, VII Syndrome:Maroteaux-Lamy (mild)(severe) | Morquio(-like)(classic) | Sanfilippo (type B)(type C)(type D)

Carence en bêta-glucoronidase Mucopolysaccharidoses, type III, IV, VI, VII Syndrome de:Maroteaux-Lamy (léger) (sévère) | Morquio (-semblable à) (classique) | Sanfilippo (type B) (type C) (type D)


Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso

maladie de Charcot-Marie-Tooth type 4B2




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'Laron-type' ->

Date index: 2021-11-07
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