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 Eponyms in category: Chromosome
 20 main and alternative entries found.
 
Alfi's syndrome
A very rare chromosome anomaly also known as monosomy 9P.
Balbiani's rings
Chromosome puffs.
Barr's body
Mass of condensed sex chromatin in the nuclei of normal female somatic cells due to inactive X chromosome.
Barr-Shaver-Carr syndrome
A chromosome XXXX syndrome with mental deficiency and variable abnormalities.
Bartholin-Patau syndrome (Thomas Bartholin)
A congenital syndrome of multiple abnormalities produced by trisomy of chromosome number 13.
Carr-Barr-Plunkett syndrome
A chromosome XXXX syndrome with mental deficiency and variable abnormalities.
Escalante's syndrome (Martin-Bell syndrome)
A syndrome comprising X-linked mental retardation in children with macroorchidism, prognathism, hypotonia and autism, and a characteristic but variable facies.
Martin Bell-Renpenning syndrome (Martin-Bell syndrome)
A syndrome comprising X-linked mental retardation in children with macroorchidism, prognathism, hypotonia and autism, and a characteristic but variable facies.
Martin-Bell syndrome
A syndrome comprising X-linked mental retardation in children with macroorchidism, prognathism, hypotonia and autism, and a characteristic but variable facies.
Morgagni-Shereshevskii-Turner-Albright syndrome (Morgagni-Turner-Albright syndrome)
Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects.
Morgagni-Turner syndrome (Morgagni-Turner-Albright syndrome)
Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects.
Morgagni-Turner-Albright syndrome
Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects.
Orbeli's syndrome (Dimitrij J. Orbeli)
Deletion of the long arm of chromosome 13 with a wide spectrum of abnormalities.
Patau syndrome (Bartholin-Patau syndrome (Thomas Bartholin))
A congenital syndrome of multiple abnormalities produced by trisomy of chromosome number 13.
Renpenning's syndrome (Martin-Bell syndrome)
A syndrome comprising X-linked mental retardation in children with macroorchidism, prognathism, hypotonia and autism, and a characteristic but variable facies.
Schereshevskii-Turner syndrome (Morgagni-Turner-Albright syndrome)
Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects.
Turner's syndrome (Morgagni-Turner-Albright syndrome)
Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects.
Turner-Albright syndrome (Morgagni-Turner-Albright syndrome)
Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects.
Turner-Vary syndrome (Morgagni-Turner-Albright syndrome)
Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects.
Ullrich-Turner syndrome (Morgagni-Turner-Albright syndrome)
Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects.
 

 
 

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