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Results 1 - 10 of 81 for black syndrome
  1. Dubin-Johnson syndrome 
    ... not show signs and symptoms of the condition. Black liver-jaundice syndrome Chronic idiopathic jaundice Chronic idiopathic jaundice with pigmented ...
    https://medlineplus.gov/genetics/condition/dubin-johnson-syndrome - Genetics
  2. 3-M syndrome 
    ... PG, Saunders E, Abu-Amero SN, Moore GE, Black GC. Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination. ...
    https://medlineplus.gov/genetics/condition/3-m-syndrome - Genetics
  3. OBSL1 gene 
    ... PG, Saunders E, Abu-Amero SN, Moore GE, Black GC. Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination. ...
    https://medlineplus.gov/genetics/gene/obsl1 - Genetics
  4. CUL7 gene 
    ... PG, Saunders E, Abu-Amero SN, Moore GE, Black GC. Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination. ...
    https://medlineplus.gov/genetics/gene/cul7 - Genetics
  5. GLI3 gene 
    ... Elson E, Perveen R, Donnai D, Wall S, Black GC. De novo GLI3 mutation in acrocallosal syndrome: broadening the phenotypic spectrum of GLI3 defects and ...
    https://medlineplus.gov/genetics/gene/gli3 - Genetics
  6. Dentatorubral-pallidoluysian atrophy 
    ... Pericak-Vance MA, Vance JM. The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family. Nat Genet. 1994 Aug;7(4):521- ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics
  7. HRAS gene 
    ... Philip N, Lacombe D, Levy N, Arveiler B, Black G. Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases. J Med ...
    https://medlineplus.gov/genetics/gene/hras - Genetics
  8. Costello syndrome 
    ... Philip N, Lacombe D, Levy N, Arveiler B, Black G. Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases. J Med ...
    https://medlineplus.gov/genetics/condition/costello-syndrome - Genetics
  9. Acrocallosal syndrome 
    ... Elson E, Perveen R, Donnai D, Wall S, Black GC. De novo GLI3 mutation in acrocallosal syndrome: broadening the phenotypic spectrum of GLI3 defects and ...
    https://medlineplus.gov/genetics/condition/acrocallosal-syndrome - Genetics
  10. Oculofaciocardiodental syndrome 
    ... Smagt JJ, Gorlin RJ, Burgess SM, Bardwell VJ, Black GC, Biesecker LG. Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR. ...
    https://medlineplus.gov/.../oculofaciocardiodental-syndrome - Genetics
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