Belongs to the group of multiple congenital anomalies/mental retardation syndromes with intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def

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syndrome de McDonough

SNOMEDCT-BE (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def / 715441004

SNOMEDCT-BE (disorder) / 715441004

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A multiple congenital anomalies/dysmorphic syndrome with characteristics of multiple skeletal malformations (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t

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syndrome de Verloove-Van Horick-Brubakk

SNOMEDCT-BE (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t / 764697003

SNOMEDCT-BE (disorder) / 764697003

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Monster NOS Multiple congenital:anomalies NOS | deformities NOS

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Anomalies multiples congénitales SAI Monstre SAI

WORLD HEALTH ORGANIZATION ICD-10: Q89.7

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A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of cerebellar-like ataxia, photosensitivity (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin

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syndrome d'ataxie-photosensibilité-petite taille

SNOMEDCT-BE (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin / 773769008

SNOMEDCT-BE (disorder) / 773769008

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Multiple congenital malformations

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Malformations congénitales multiples

WORLD HEALTH ORGANIZATION ICD-10: Q89.7

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

diaphyseal aclasis [ multiple exostoses ]

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maladie exostosante [ maladie ostéogénique | maladie de Bessel-Hagen | chondrodysplasie déformante héréditaire | maladie des exostoses multiples ]

Bones and Joints

Os et articulations

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arthrogryposis multiplex congenita [ amyoplasia congenita | myodystrophia fetalis | congenital multiple arthrogryposis ]

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arthrogrypose congénitale multiple [ amyoplasie congénitale | arthrogryposis multiplex congénitale | raideur articulaire congénitale | arthrogrypose | myodystrophie foetale ]

Bones and Joints | Musculoskeletal System | Symptoms (Medicine)

Os et articulations | Appareil locomoteur (Médecine) | Symptômes (Médecine)

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Others have searched : bessel-hagen disease monster nos multiple congenital anomalies nos multiple congenital exostoses multiple congenital malformations amyoplasia congenita arthrogryposis multiplex congenita congenital multiple arthrogryposis deformities nos diaphyseal aclasis hereditary deforming chondrodysplasia hereditary multiple exostosis multiple cartilaginous exostoses multiple exostoses multiple exostosis multiple osteochondromas myodystrophia fetalis

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'multiple congenital exostoses'

Date index:2022-12-24 -

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Translation of "multiple congenital exostoses " (English → French) :

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