Category:CHARGE syndrome

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<nowiki>Síndrome de CHARGE; CHARGE症候群; syndrome CHARGE; CHARGE sendromu; chargesyndrom; Asocjacja CHARGE; sindrome CHARGE; Síndrome de CHARGE; Синдром CHARGE; Síndrome CHARGE; CHARGE-Syndrom; Charge-oireyhtymä; CHARGE syndrome; متلازمة تشارج; CHARGE聯合畸形; CHARGE syndrom; syndrome that is characterized by a pattern of congenital anomalies including choanal atresia and malformations of the heart, inner ear, and retina; 先天性疾患; Syndrom; Sindrome de CHARGE; C.H.A.R.G.E; Syndrome de CHARGE; Syndrome de charge; Hall-Hittner; Charge-Syndrom; CHARGE-Assoziation; Associação CHARGE; CHARGE association; Coloboma-heart defects-atresia choanae-retardation of growth and development-genitourinary problems-ear abnormalities syndrome; CHARGE SYNDROME; Coloboma, Heart Defects, Choanal Atresia, Retardation of Growth and Development, Genital Abnormalities, and Ear Anomalies Association; Hall-Hittner syndrome; Coloboma, Heart Malformation, Choanal Atresia, Retardation of Growth and Development, Genital Abnormalities, and Ear Malformations (CHARGE) Association; Charge Association--Coloboma, Heart Anomaly, Choanal Atresia, Retardation, Genital and Ear Anomalies; Zespół CHARGE; Zespół Halla-Hittnera; CHARGE-syndrooma; Charge-syndrooma; CHARGE-oireyhtymä; CHARGE syndrom; Charge syndrom</nowiki>
CHARGE syndrome 
syndrome that is characterized by a pattern of congenital anomalies including choanal atresia and malformations of the heart, inner ear, and retina
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Subclass of
  • syndrome
  • immunodeficiency due to absence of thymus
  • syndromic genetic deafness
  • rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism
  • syndromic renal or urinary tract malformation
  • lens shape anomaly
  • multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
  • syndromic developmental defect of the eye
  • syndrome or malformation associated with head and neck malformations
  • rare syndrome with cardiac malformations
  • syndromic urogenital tract malformation
  • rare abdominal surgical disease
  • rare genetic bone disease
  • disease
Authority file
Wikidata Q1023604
BabelNet ID: 01945337n
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