SE-ATLAS

Syndrome de cataracte-glaucome Cataracte coralliforme Cataracte totale précoce Alpha-mannosidose de l'adulte Syndrome de Marinesco-Sjögren Syndrome de Marshall Syndrome de Meckel Syndrome de Hallermann-Streiff Alpha-mannosidose Syndrome de Hallermann-Streiff-like Syndrome de délétion 21q Syndrome d'Alport Syndrome d'Alström Déficit en alpha-N-acétylgalactosaminidase Amaurose congénitale de Leber Syndrome de Harrod Déficit multiple en sulfatases Syndrome muscle-oeil-cerveau Aniridie Syndrome de crâne en trèfle-anomalies congénitales multiples Nanisme microcéphalique primordial type Toriello Pseudopseudohypoparathyroïdie Trichothiodystrophie Pseudohypoparathyroïdie type 1C Syndrome d'Apert Lipidose avec surcharge en triglycérides et ichtyose Myopathie myotonique proximale Syndrome de Siegler-Brewer-Carey Déficience intellectuelle liée à l'X type Najm Syndrome de spasmes infantiles-pouces larges Syndrome de Nathalie Acidurie 3-méthylglutaconique type 7 Cataracte lamellaire précoce Syndrome neuro-musculo-squelettique type chypriote Syndrome DOORS Dysplasie oculo-dento-digitale Syndrome oculo-facio-cardio-dentaire Syndrome oculo-palato-cérébral Duplication non distale 10q Syndrome oculo-cérébral d'hypopigmentation, type Cross Syndrome de surdité-onychodystrophie Syndrome oculo-cérébral d'hypopigmentation, type Preus Syndrome de dégénérescence cochléo-sacculaire-cataracte Syndrome d'hyperferritinémie-cataracte héréditaire Syndrome d'anomalie de l'oeil-arachnodactylie-cardiopathie Cataracte polaire postérieure précoce Chondrodysplasie ponctuée rhizomélique Cataracte partielle précoce Cataracte zonulaire précoce Dysplasie ostéodysplasique microcéphalique type Saul-Wilson Syndrome MRCS Hypoparathyroïdie isolée familiale Hypoparathyroïdie isolée familiale due à l'agénésie de la glande parathyroïde Syndrome de Parkes Weber Syndrome de Peters plus Syndrome de Klippel-Trénaunay Syndrome d'hypoplasie nasale et oculaire-hypogonadisme hypogonadotrope Spondylo-oculaire syndrome Microphtalmie avec anomalies cérébrales et des mains Trisomie 5p Syndrome d'ostéogenèse imparfaite-microcéphalie-cataracte Syndrome de cataracte congénitale-hépatopathie néonatale sévère-retard global de développement Chondrodysplasie ponctuée rhizomélique type 5 Syndrome tricho-rétino-dento-digital Syndrome Aymé-Gripp Déficit érythrocytaire en galactose épimérase Chondrodysplasie létale de Blomstrand Syndrome familial de dystrophie rétinienne progressive-colobome-cataracte congénitale Syndrome d'anomalies du développement-surdité-dystonie Maladie de Refsum Rétinoschisis lié à l'X Syndrome de Schwartz-Jampel Dysplasie mucoépithéliale héréditaire Syndrome de Smith-Lemli-Opitz Syndrome de Sotos Syndrome de Stickler Duplication distale 2p Syndrome de dystrophie musculaire congénitale-cataracte infantile-hypogonadisme Maladie musculo-squelettique avec cataracte Syndrome d'ectopie du cristallin-dystrophie choriorétinienne-myopie Syndrome de microduplication 3q26 Trisomie 21 Syndrome létal de non-compaction ventriculaire gauche-convulsions-hypotonie-cataracte-retard de développement Duplication distale 10q Syndrome de microcéphalie-brachydactylie-déficience intellectuelle Syndrome de cataracte-déficience intellectuelle-hypogonadisme Syndrome de Turner Syndrome WAGR Syndrome de Werner Galactosémie classique Homocystinurie par déficit en cystathionine bêta-synthase Xeroderma pigmentosum Syndrome de De Barsy Syndrome Proteus-like Monosomie X Atrophie gyrée choriorétinienne Maladie de Sanfilippo type A Maladie de Sanfilippo type B Maladie de Sanfilippo type D Déficit en alpha-N-acétyl-galactosaminidase type 3 Anomalies du membre supérieur, de l'oeil et de l'oreille Syndrome oculo-squeletto-dentaire Syndrome micro Incontinentia pigmenti ALG8-CDG Microcephaly-microcornea syndrome, Seemanova type 3-methylglutaconic aciduria type 4 Juvenile cataract-microcornea-renal glucosuria syndrome Congenital-onset Steinert myotonic dystrophy X-linked Alport syndrome-diffuse leiomyomatosis Stickler syndrome type 1 Aniridia-intellectual disability syndrome Neonatal adrenoleukodystrophy Rhizomelic chondrodysplasia punctata type 3 Monosomy 18p Galactose mutarotase deficiency Monosomy 18q 2q24 microdeletion syndrome Pseudohypoparathyroidism type 1A Turner syndrome due to structural X chromosome anomalies Early-onset posterior subcapsular cataract Autosomal recessive Stickler syndrome Autosomal dominant deafness-onychodystrophy syndrome Autosomal recessive cerebelloparenchymal disorder type 3 Early-onset sutural cataract Pulverulent cataract Cerulean cataract Early-onset anterior polar cataract Early-onset nuclear cataract Foveal hypoplasia-presenile cataract syndrome Crouzon syndrome Distal triplication 15q 15q overgrowth syndrome Congenital cataract microcornea with corneal opacity Osteoporosis-pseudoglioma syndrome Blau syndrome Tetraamelia-multiple malformations syndrome Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome Lymphedema-distichiasis syndrome Trisomy 9p Tetrasomy 5p Generalized galactose epimerase deficiency PYCR1-related De Barsy syndrome Absence deformity of leg-cataract syndrome Wolf-Hirschhorn syndrome Monosomy 5p X-linked intellectual disability, Armfield type Congenital cataract-hearing loss-severe developmental delay syndrome Congenital rubella syndrome Congenital varicella syndrome Angioosteohypertrophic syndrome Congenital cataracts-facial dysmorphism-neuropathy syndrome Triploidy Trisomy 18 Epidermal nevus syndrome Erythrokeratodermia variabilis Cardiomyopathy-cataract-hip spine disease syndrome Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Metabolic disease with cataract Autosomal recessive Alport syndrome Intellectual disability-cataracts-kyphosis syndrome Cardiac disease with cataract Autosomal recessive palmoplantar keratoderma and congenital alopecia Autosomal dominant Alport syndrome Dentocutaneous disease with cataract Cataract-ataxia-deafness syndrome Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome Rothmund-Thomson syndrome type 2 Craniofacial anomaly with cataract Rothmund-Thomson syndrome Cataract-aberrant oral frenula-growth delay syndrome Cataract-hypertrichosis-intellectual disability syndrome Galactosemia Cataract-nephropathy-encephalopathy syndrome Autoimmune polyendocrinopathy type 1 Intellectual disability-cataracts-calcified pinnae-myopathy syndrome Microspherophakia-metaphyseal dysplasia syndrome Syndromic cataract Childhood-onset Steinert myotonic dystrophy Mucopolysaccharidosis type 3 Multiple epiphyseal dysplasia, Beighton type Hypomyelination-congenital cataract syndrome Hidrotic ectodermal dysplasia Relapsing polychondritis Microcephaly-congenital cataract-psoriasiform dermatitis syndrome Steinert myotonic dystrophy Trisomy 13 Renal disease with cataract Cataract-microcornea syndrome Early-onset non-syndromic cataract Hypergonadotropic hypogonadism-cataract syndrome Vogt-Koyanagi-Harada disease Hydrocephaly-cerebellar agenesis syndrome Galactokinase deficiency Galactose epimerase deficiency Cerebrotendinous xanthomatosis Zellweger syndrome Mandibuloacral dysplasia Mosaic monosomy X Fatty acyl-CoA reductase 1 deficiency Sanfilippo syndrome type C Monosomy 13q34 Autosomal dominant hypocalcemia CODAS syndrome COFS syndrome Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Adams-Oliver syndrome Vici syndrome ALG2-CDG Lathosterolosis Scalp-ear-nipple syndrome Flynn-Aird syndrome Late-onset Steinert myotonic dystrophy Juvenile-onset Steinert myotonic dystrophy Nance-Horan syndrome Cataract-congenital heart disease-neural tube defect syndrome Craniolenticulosutural dysplasia Norrie disease Congenital muscular dystrophy, Fukuyama type ALDH18A1-related De Barsy syndrome Systemic disease with cataract Rothmund-Thomson syndrome type 1 X-linked Alport syndrome Basel-Vanagaite-Smirin-Yosef syndrome Pseudohypoparathyroidism with Albright hereditary osteodystrophy Spastic paraparesis-cataracts-speech delay syndrome Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome Adult-onset Steinert myotonic dystrophy Familial isolated hypoparathyroidism due to impaired PTH secretion Dahlberg-Borer-Newcomer syndrome Roberts syndrome Rhizomelic chondrodysplasia punctata type 2 Isolated aniridia Monosomy 13q14 Distal deletion 13q Autosomal dominant spastic paraplegia type 9A Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract Deafness-intellectual disability syndrome, Martin-Probst type Cataract-intellectual disability-anal atresia-urinary defects syndrome X-linked dominant chondrodysplasia punctata Persistent hyperplastic primary vitreous Cataract-deafness-hypogonadism syndrome Spastic ataxia-corneal dystrophy syndrome Abetalipoproteinemia Oculocerebrorenal syndrome of Lowe Rhizomelic chondrodysplasia punctata type 1 Mosaic variegated aneuploidy syndrome Mevalonic aciduria Stickler syndrome type 2 Alpha-mannosidosis, infantile form Chromosomal anomaly with cataract Cerebral disease with cataract