Create issue ticket

651 Possible Causes for Lujan-Fryns Syndrome

  • Mesoaxial Synostotic Syndactyly with Phalangeal Reduction

    syndrome Limb-mammary syndrome Lissencephaly Lissencephaly, X-linked Lujan-Fryns syndrome Lymphedema-distichiasis syndrome Mandibular hypoplasia, deafness, progeroid features[qlinics.com] Lissencephaly type 2 (Norman-Roberts type) RELN Lissencephaly type 3 TUBA1A Lissencephaly type 5 LAMB1 Lissencephaly, X-linked type 1 DCX Lissencephaly, X-linked type 2 ARX Lujan-Fryns[centogene.com] […] adducted thumbs (MASA) syndrome, Spastic MED12 FG syndrome, Lujan-Fryns syndrome, Mental retardation, with Marfanoid habitus, Ohdo syndrome, Opitz-Kaveggia syndrome MLC1[genda.com.ar]

  • Organic Personality Disorder

    — Classification and external resources … Wikipedia Lujan-Fryns syndromeLujanFryns syndrome Classification and external resources LujanFryns syndrome in a young adult[medicine.academic.ru] Like other ASD forms, Asperger syndrome is characterized by impairment in social interaction accompanied by restricted and repetitive interests … Wikipedia Asperger syndrome[medicine.academic.ru]

  • Craniorhiny

    Syndrome Lujan Fryns syndrome Malpuech facial clefting syndrome Mandibuloacral dysplasia with type B lipodystrophy Mandibulofacial Dysostosis Syndrome, Bauru Type Mandibulofacial[ctdbase.org] Lujan Fryns Syndrome Macrocephaly Mandibuloacral Dysplasia with Type B Lipodystrophy Mandibulofacial Dysostosis Syndrome, Bauru Type Mandibulofacial Dysostosis with Macroblepharon[rgd.mcw.edu] Keppen-Lubinsky Syndrome Kleefstra syndrome Klippel-Feil syndrome KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM Kosztolanyi Syndrome[rgd.mcw.edu]

  • Hirschsprung Disease Type D-Brachydactyly Syndrome

    Lissencephaly type 2 (Norman-Roberts type) RELN Lissencephaly type 3 TUBA1A Lissencephaly type 5 LAMB1 Lissencephaly, X-linked type 1 DCX Lissencephaly, X-linked type 2 ARX Lujan-Fryns[centogene.com] Liver Glycogenosis, Type I Liver Glycogenosis, Type II Lujan-Fryns Syndrome Lymphangioleiomyomatosis Lymphoedema, Hereditary Lymphoedema-distichiasis Syndrome Macrocephaly[sequencing.com] 4 6 Long QT Syndrome 5 5 Long QT Syndrome 6 5 Long QT Syndrome 9 7 Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency 5 Lowe Syndrome 3 Lujan-Fryns Syndrome 4 Lung Cancer[preventiongenetics.com]

  • Renpenning Syndrome

    Lujan-Fryns syndrome Fragile x syndrome[en.wikipedia.org] FG syndrome-1; Lujan-Fryns syndrome XLR 20 MID1 300552 Opitz GBBB syndrome, X-linked XLR 6 NHS 300457 Nance-Horan syndrome XL, XLD 8 NIPBL 608667 Cornelia de Lange syndrome[centogene.com] Leigh Syndrome Lenz Microphthalmia Syndrome LEOPARD Syndrome Lesch-Nyhan Syndrome (LNS) Li-Fraumeni Syndrome (LFS) Lissencephaly Lowe Syndrome Lujan-Fryns Syndrome Lymphedema-Distichiasis[corp.credoreference.com]

  • Autosomal Recessive Spastic Paraplegia Type 27

    Syndrome Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome Lujan-Fryns Syndrome Luscan-Lumish Syndrome Mental Retardation, Autosomal Dominant 27 Mental Retardation[familydiagnosis.com] Flat Face-Microstomia-Ear Anomaly Syndrome Glass Syndrome Grix-Blankenship-Peterson Syndrome Harrod Syndrome Hennekam-Beemer Syndrome Hydrocephaly-Low Insertion Umbilicus[familydiagnosis.com] […] include: 1 Causes of Long Nose : 16p11.2p12.2 Microdeletion Syndrome Acromegaloid Facial Appearance Syndrome Alagille Syndrome Alagille Syndrome 1 Beaulieu-Boycott-Innes Syndrome[familydiagnosis.com]

  • Ochoa Syndrome

    The Lujan-Fryns syndrome affects predominantly males.[ojrd.biomedcentral.com] JP, Peuskens J: Lujan-Fryns syndrome in the differential diagnosis of schizophrenia.[ojrd.biomedcentral.com] Keywords Pectus Excavatum FMR1 Gene Narrow Face Moderate Mental Retardation Prominent Forehead Disease name/synonyms Lujan syndrome Lujan-Fryns syndrome X-linked mental retardation[ojrd.biomedcentral.com]

  • Dilated Cardiomyopathy Type 2B

    […] of Lowe Lujan-Fryns syndrome 309520 MED12 mediator complex subunit 12 Lumbar disc herniation, susceptibility to 603932 COL11A1 collagen, type XI, alpha 1 Lymphangioleiomyomatosis[ac-gen.com] MED12 Synonym(s): ARC240; CAGH45; FGS1; HOPA; MED12S; OHDOX; OKS; OPA1; TNRC11; TRAP230 The MED12 gene is associated with X-linked recessive Lujan-Fryns syndrome ( LFS ) ([invitae.com] 4 6 Long QT Syndrome 5 5 Long QT Syndrome 6 5 Long QT Syndrome 9 7 Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency 5 Lowe Syndrome 3 Lujan-Fryns Syndrome 4 Lung Cancer[preventiongenetics.com]

  • Micrognathism

    Lathosterolosis Lethal congenital contracture syndrome Lethal restrictive dermopathy Loeys-Dietz syndrome Lujan-Fryns syndrome Marden-Walker syndrome Marfan's syndrome Micrognathia[wikidoc.org] See also Lujan-Fryns syndrome Fragile x syndrome Renpenning syndrome is an X-linked intellectual disability syndrome (XLMR, see this term) characterized by intellectual deficiency[findzebra.com] Fetal akinesia-hypokinesia sequence Fetal aminopterin-like syndrome Hurst's microtia-absent patellae-micrognathia syndrome Juvenile chronic arthritis Kyphomelic dysplasia[wikidoc.org]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    MED12 gene Lujan-Fryns syndrome Opitz-Kaveggia syndrome, also known as FG syndrome-1 MFRP gene Posterior microphthalmia, retinitis pigmentosa, foveoschisis, and optic disc[julesberman.blogspot.com] Legius syndrome Intellectual Disability LEOPARD syndrome Intellectual Disability Lujan-Fryns syndrome Intellectual Disability Mabry syndrome Intellectual Disability MACS[genomediagnosticsnijmegen.nl] […] adducted thumbs (MASA) syndrome, Spastic MED12 FG syndrome, Lujan-Fryns syndrome, Mental retardation, with Marfanoid habitus, Ohdo syndrome, Opitz-Kaveggia syndrome MLC1[genda.com.ar]

Further symptoms