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197 Possible Causes for Opitz-Frias Syndrome

  • Laryngo-Tracheo-Esophageal Cleft

    Laryngeal cleft can also be a component of other genetic syndromes, including Pallister-Hall syndrome and G syndrome (Opitz-Frias syndrome).[en.wikipedia.org] OPITZ-FRIAS SYNDROME 13. POTTER SEQUENCE OR SYNDROME 14. SCHISIS ASSOCIATION 15. SIRENOMELIA SEQUENCE 16. TRACHEALAGENESIS ASSOCIATION 17.[tefvater.org] syndrome Pallister-Hall syndrome DiGeorgesyndrome CHARGE syndrome VACTERL association OPITZ-FRIAS SYNDROME X-linked or autosomal dominant 1:4,000 to 1:100,000 22q11.2 microdeletionsyndrome[laryngeal-cleft.com]

  • Fitzsimmons-McLachlan-Gilbert Syndrome

    , Freiberg's disease, Freire maia pinheiro opitz syndrome, Frey's syndrome, Frias syndrome, Fried syndrome, Fried-Goldberg-Mundel syndrome, Friedman goodman syndrome, Friedreich[yumpu.com] Maia Pinheiro Opitz syndrome Frenkel Russe syndrome Frey's syndrome Frias syndrome Fried Goldberg Mundel syndrome Friedel Heid Grosshans syndrome Friedman Goodman syndrome[bioreference.net] Freire Maia odontotrichomelic syndrome[?] Freire Maia Pinheiro Opitz syndrome[?] Frenkel Russe syndrome[?] Frey's syndrome[?] Frias syndrome[?][encyclopedia.kids.net.au]

  • Larynx Atresia

    Associated Abnormalities with Laryngeal Atresia reported in the Literature * Name of Syndrome Mode of Inheritance Fraser syndrome Autosomal Recessive OpitzFrias syndrome[fetalsono.com] Laryngeal Clefts Rare congenital anomaly Congenital laryngeal anomaly occurs in 1 in 2000 live births 0.3% are laryngeal clefts Boy:Girl… 5:3 ratio Associated with VACTERL, Opitz-Frias[laryngeal-cleft.com] syndrome, Pallister-Hall syndrome Embryology of Larynx Respiratory primordium develop from diverticulum on foregut Tracheobronchial groove arise on either side and fuse in[laryngeal-cleft.com]

  • Benign Adult Familial Myoclonic Epilepsy

    , Opitz BBBG syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, hypertelorism with esophageal abnormalities and hypospadias Osteopetrose ( 1 Files ) Erkrankung[orphananesthesia.eu] G/BBB Syndrom ( 1 Files ) Erkrankung : Opitz G/BBB Syndrom ICD 10: Q87.8 Synonyme : Hypertelorism-hypospadias syndrome, hypospadias-dysphagia syndrome, OpitzBBB/G syndrome[orphananesthesia.eu] […] infantile, lateinfantile, juvenile or adult onset and associated with names of investigators such as Santavuori-Haltia, Jansky-Bielschowsky, Batten, Spielmeyer-Vogt, Kufs Opitz[orphananesthesia.eu]

  • Micrognathism

    […] acrofacial dysostosis Noonan's syndrome Opitz-Frias syndrome Orofaciodigital syndrome type 4 Otopalatodigital syndrome type 2 Pallister-Hall syndrome Pierre Robin syndrome[wikidoc.org] Lethal restrictive dermopathy Loeys-Dietz syndrome Lujan-Fryns syndrome Marden-Walker syndrome Marfan's syndrome Micrognathia with peromelia Miller-Dieker syndrome Nager[wikidoc.org] Postaxial acrofacial dysostosis syndrome Rothmund-Thomson syndrome Schwartz-Jampel-Aberfeld syndrome Scott craniodigital syndrome Smith-Lemli-Opitz syndrome Syphilis, congenital[wikidoc.org]

  • Distal Spinal Muscular Atrophy Type 3

    , Opitz BBBG syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, hypertelorism with esophageal abnormalities and hypospadias Osteopetrose ( 1 Files ) Erkrankung[orphananesthesia.eu] G/BBB Syndrom ( 1 Files ) Erkrankung : Opitz G/BBB Syndrom ICD 10: Q87.8 Synonyme : Hypertelorism-hypospadias syndrome, hypospadias-dysphagia syndrome, OpitzBBB/G syndrome[orphananesthesia.eu] […] infantile, lateinfantile, juvenile or adult onset and associated with names of investigators such as Santavuori-Haltia, Jansky-Bielschowsky, Batten, Spielmeyer-Vogt, Kufs Opitz[orphananesthesia.eu]

  • Isolated Congenital Alacrima

    The G (Opitz-Frias) syndrome is also an autosomal dominant disorder characterised by hypertelorism, hypospadias, stridor, and dysphagia.[link.springer.com] The National Foundation-March of Dimes, New York, pp 86–94 Google Scholar Opitz JM, Frias JL, Gutenberg JE, Pellet JR (1969b) The G syndrome of multiple congenital anomalies[link.springer.com] Malformation syndromes, vol 5, part 2.[link.springer.com]

  • Kasabach Merritt Syndrome

    , Opitz BBBG syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, hypertelorism with esophageal abnormalities and hypospadias Osteopetrose ( 1 Files ) Erkrankung[orphananesthesia.eu] G/BBB Syndrom ( 1 Files ) Erkrankung : Opitz G/BBB Syndrom ICD 10: Q87.8 Synonyme : Hypertelorism-hypospadias syndrome, hypospadias-dysphagia syndrome, OpitzBBB/G syndrome[orphananesthesia.eu] […] infantile, lateinfantile, juvenile or adult onset and associated with names of investigators such as Santavuori-Haltia, Jansky-Bielschowsky, Batten, Spielmeyer-Vogt, Kufs Opitz[orphananesthesia.eu]

  • Hypospadias

    Opitz-Frias syndrome, G syndrome, Opitz-G syndrome, type 2, Hypertelorism hypospadias syndrome, Hypertelorism with esophageal abnormality and hypospadias, BBB syndrome, Telecanthus[rarediseases.info.nih.gov] Noonan syndrome 2 Synonyms: NS2, Noonan syndrome autosomal recessive, Autosomal recessive Noonan syndrome Opitz G/BBB syndrome Synonyms: Hypospadias-dysphagia, syndrome,[rarediseases.info.nih.gov] […] with levocardia, Isolated levocardia with situs inversus Mulibrey Nanism Synonyms: Muscle-liver-brain-eye nanism, Pericardial constriction and growth failure, Perheentupa syndrome[rarediseases.info.nih.gov]

  • Distal Myopathy Type 3

    , Opitz BBBG syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, hypertelorism with esophageal abnormalities and hypospadias Osteopetrose ( 1 Files ) Erkrankung[orphananesthesia.eu] , Opitz BBBG syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, hypertelorism with esophageal abnormalities and hypospadias Osteopetrosis ( 1 Files ) Disease[orphananesthesia.eu] G/BBB Syndrom ( 1 Files ) Erkrankung : Opitz G/BBB Syndrom ICD 10: Q87.8 Synonyme : Hypertelorism-hypospadias syndrome, hypospadias-dysphagia syndrome, OpitzBBB/G syndrome[orphananesthesia.eu]

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