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'en:immunoglobulin superfamily member 1 deficiency syndrome'
(id=9097905 ; fe=en:immunoglobulin superfamily member 1 deficiency syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=587 creation date=2017-10-27 touchdate=2025-07-16 16:07:43.000)
≈ 19 relations sortantes

  1. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 28 / 1 -> en:hypothyroidism, central, and testicular enlargement
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:hypothyroidism, central, and testicular enlargement | rel=r_associated | relid=0 | w=28
  2. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 26 / 0.929 -> immunoglobuline
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=immunoglobuline | rel=r_associated | relid=0 | w=26
  3. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 26 / 0.929 -> syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=syndrome | rel=r_associated | relid=0 | w=26
  4. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 25 / 0.893 -> en:immunoglobulin
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:immunoglobulin | rel=r_associated | relid=0 | w=25
  5. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:10p13-p14 deletion syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:10p13-p14 deletion syndrome | rel=r_associated | relid=0 | w=20
  6. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:autoimmune polyglandular syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:autoimmune polyglandular syndrome | rel=r_associated | relid=0 | w=20
  7. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:autosomal dominant congenital deafness with onychodystrophy
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:autosomal dominant congenital deafness with onychodystrophy | rel=r_associated | relid=0 | w=20
  8. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:chromosome 16p12.1 deletion syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:chromosome 16p12.1 deletion syndrome | rel=r_associated | relid=0 | w=20
  9. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:cortical dysplasia-focal epilepsy syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
  10. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:insulin receptor mutation - associated insulin resistance syndromes
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:insulin receptor mutation - associated insulin resistance syndromes | rel=r_associated | relid=0 | w=20
  11. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:kenny-caffey syndrome type 2
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:kenny-caffey syndrome type 2 | rel=r_associated | relid=0 | w=20
  12. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:maternal diabetes and deafness syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:maternal diabetes and deafness syndrome | rel=r_associated | relid=0 | w=20
  13. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:mullerian-renal-cervical spine syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:mullerian-renal-cervical spine syndrome | rel=r_associated | relid=0 | w=20
  14. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:multiple vascular disruption syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:multiple vascular disruption syndrome | rel=r_associated | relid=0 | w=20
  15. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:single central incisor syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:single central incisor syndrome | rel=r_associated | relid=0 | w=20
  16. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:triple a syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:triple a syndrome | rel=r_associated | relid=0 | w=20
  17. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:Triple a syndrome
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:Triple a syndrome | rel=r_associated | relid=0 | w=20
  18. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:wilms tumor 1 gene syndromes
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:wilms tumor 1 gene syndromes | rel=r_associated | relid=0 | w=20
  19. en:immunoglobulin superfamily member 1 deficiency syndrome -- r_associated #0: 20 / 0.714 -> en:x- linked recessive
    n1=en:immunoglobulin superfamily member 1 deficiency syndrome | n2=en:x- linked recessive | rel=r_associated | relid=0 | w=20
≈ 20 relations entrantes

  1. en:Triple a syndrome --- r_associated #0: 38 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:Triple a syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=38
  2. en:insulin receptor mutation - associated insulin resistance syndromes --- r_associated #0: 35 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:insulin receptor mutation - associated insulin resistance syndromes | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=35
  3. en:kenny-caffey syndrome type 2 --- r_associated #0: 35 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:kenny-caffey syndrome type 2 | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=35
  4. en:triple a syndrome --- r_associated #0: 35 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:triple a syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=35
  5. en:single central incisor syndrome --- r_associated #0: 34 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:single central incisor syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=34
  6. en:x- linked recessive --- r_associated #0: 32 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:x- linked recessive | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=32
  7. en:cortical dysplasia-focal epilepsy syndrome --- r_associated #0: 29 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=29
  8. en:maternal diabetes and deafness syndrome --- r_associated #0: 29 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:maternal diabetes and deafness syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=29
  9. en:mullerian-renal-cervical spine syndrome --- r_associated #0: 29 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:mullerian-renal-cervical spine syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=29
  10. en:wilms tumor 1 gene syndromes --- r_associated #0: 29 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:wilms tumor 1 gene syndromes | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=29
  11. en:autoimmune polyglandular syndrome --- r_associated #0: 28 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:autoimmune polyglandular syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=28
  12. en:10p13-p14 deletion syndrome --- r_associated #0: 27 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:10p13-p14 deletion syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=27
  13. en:chromosome 16p12.1 deletion syndrome --- r_associated #0: 27 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:chromosome 16p12.1 deletion syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=27
  14. en:hypothyroidism, central, and testicular enlargement --- r_associated #0: 27 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:hypothyroidism, central, and testicular enlargement | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=27
  15. en:multiple vascular disruption syndrome --- r_associated #0: 27 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:multiple vascular disruption syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=27
  16. en:autosomal dominant congenital deafness with onychodystrophy --- r_associated #0: 26 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:autosomal dominant congenital deafness with onychodystrophy | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=26
  17. immunoglobuline --- r_associated #0: 20 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=immunoglobuline | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=20
  18. syndrome --- r_associated #0: 20 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=syndrome | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=20
  19. en:immunoglobulin --- r_associated #0: 10 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=en:immunoglobulin | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=10
  20. syndromes du gène 1 de la tumeur de Wilms --- r_associated #0: 5 --> en:immunoglobulin superfamily member 1 deficiency syndrome
    n1=syndromes du gène 1 de la tumeur de Wilms | n2=en:immunoglobulin superfamily member 1 deficiency syndrome | rel=r_associated | relid=0 | w=5
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contact: mathieu.lafourcade@lirmm.fr