SE-ATLAS

Goldenhar-Syndrom Pfeiffer-Syndrom Typ 1 Pfeiffer-Syndrom Typ 3 Pfeiffer-Syndrom Typ 2 Crouzon-Syndrom - Acanthosis nigricans Otorhinolaryngologische Krankheit, seltene Nager-Syndrom Enzephalozele, isolierte Oto-spondylo-megaepiphysäre Dysplasie, autosomal-dominante Osteosklerose-Entwicklungsverzögerung-Kraniosynostose-Syndrom Atelosteogenesis Typ II Saethre-Chotzen-Syndrom Atelosteogenesis Typ III Kleeblattschädel - multiple kongenitale Anomalien Dysplasie, fronto-nasale Holoprosenzephalie-Kraniosynostose-Syndrom Isotretinoin-Syndrom Kraniosynostose - Hydrozephalus - Chiari-Fehlbildung I - radioulnare Synostose Dobrow-Syndrom Akrozephalosyndaktylie Familiäre lambdoide Synostose Kraniosynostose, nicht-syndromale Fetale Valproat-Spektrumstörung SCARF-Syndrom Baller-Gerold-Syndrom Seltene Krankheit der Maxillo-fazialen Chirurgie Aminopterin/Methotrexat-Embryopathie Kraniosynostose, syndromale Indometacin-Embryopathie Smith-Lemli-Opitz-Syndrom Intelligenzminderung-Brachydaktylie-Pierre Robin-Syndrom Jodmangelsyndrom, fetales Smith-Magenis-Syndrom Kokain-Embryofetopathie Dihydantoin-Embryopathie Kabuki-Syndrom Trimethadion-Embryopathie Vitamin K-Antagonisten-Embryopathie Fetales Alkoholsyndrom Letal okzipitale Enzephalozele-Skelettdysplasie-Syndrom Shprintzen-Goldberg-Syndrom Methylquecksilber-Embryopathie Cardiocranial syndrome, Pfeiffer type Fetal minoxidil syndrome Phenobarbital embryopathy Stickler syndrome Toluene embryopathy Methimazole embryofetopathy Cranioectodermal dysplasia Pierre Robin syndrome associated with collagen disease Non-syndromic bilambdoid and sagittal craniosynostosis Diabetic embryopathy Cantú syndrome Pierre Robin syndrome associated with a chromosomal anomaly Teebi-Shaltout syndrome Frontofacionasal dysplasia Rare disease with Pierre Robin syndrome SPECC1L-related hypertelorism syndrome Isolated oxycephaly Carpenter syndrome Craniofrontonasal dysplasia Autosomal recessive Stickler syndrome Craniofrontonasal dysplasia-Poland anomaly syndrome Oculomaxillofacial dysostosis 22q11.2 deletion syndrome TARP syndrome Fetal parvovirus syndrome Craniomicromelic syndrome Pierre Robin syndrome associated with branchial archs anomalies Isolated cloverleaf skull syndrome Oculoauriculofrontonasal syndrome Pierre Robin syndrome associated with bone disease Dysostosis with predominant craniofacial involvement Craniosynostosis, Philadelphia type Maternal phenylketonuria Craniotelencephalic dysplasia Pfeiffer syndrome Frontorhiny Teratogenic Pierre Robin syndrome Craniosynostosis-cataract syndrome Waardenburg syndrome Craniosynostosis Pseudoaminopterin syndrome Craniosynostosis-fibular aplasia syndrome Maternal hyperthermia-induced birth defects X-linked intellectual disability-plagiocephaly syndrome Craniosynostosis-dysmorphism-brachydactyly syndrome Isolated Pierre Robin syndrome Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome Familial scaphocephaly syndrome Jackson-Weiss syndrome Craniosynostosis, Boston type Non-syndromic sagittal craniosynostosis Familial osteodysplasia, Anderson type Craniosynostosis-dental anomalies Familial scaphocephaly syndrome, McGillivray type Treacher-Collins syndrome Isolated plagiocephaly Non-syndromic bicoronal craniosynostosis Cloverleaf skull-asphyxiating thoracic dysplasia syndrome Curry-Jones syndrome Acromelic frontonasal dysplasia Rare sucking/swallowing disorder Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome Goodman syndrome Cornelia de Lange syndrome Frontonasal dysplasia-alopecia-genital anomalies syndrome Crouzon syndrome Summitt syndrome Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome Craniolenticulosutural dysplasia Kniest dysplasia Muenke syndrome C syndrome Antley-Bixler syndrome Pai syndrome Apert syndrome Rare neoplastic disease Syndrome de craniosynostose-calcifications intracrâniennes Syndrome de Stickler type 2 Syndrome de dysostose mandibulo-faciale-macroblépharon-macrostomie Syndrome cranio-facio-fronto-digital Syndrome de l'X fragile Syndrome de Stickler type 1 Hyperplasie congénitale des surrénales par déficit en cytochrome P450 oxydoréductase Syndrome de Lowry-MacLean Encéphalocèle nasale Syndrome de trigonocéphalie-anomalies des extrémités Syndrome de craniosynostose-anomalies anales-porokératose Craniosynostose métopique non syndromique Spectre oculo-auriculo-vertébral avec anomalies radiales Syndrome de Hunter-McAlpine Syndrome de trigonocéphalie-petite taille-retard de croissance Acro-céphalo-polydactylie Atélostéogenèse type I Craniosynostose de Herrmann-Opitz Syndrome des synostoses multiples