'en:acatalasia'
(id=9966033 ; fe=en:acatalasia ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=1261 creation date=2018-02-20 touchdate=2025-11-02 07:58:42.000) ≈ 40 relations sortantes
- en:acatalasia --
r_associated #0: 49 / 1 ->
acatalasémie
n1=en:acatalasia | n2=acatalasémie | rel=r_associated | relid=0 | w=49
- en:acatalasia --
r_associated #0: 48 / 0.98 ->
en:acatalasemia
n1=en:acatalasia | n2=en:acatalasemia | rel=r_associated | relid=0 | w=48
- en:acatalasia --
r_associated #0: 44 / 0.898 ->
maladie de Takahara
n1=en:acatalasia | n2=maladie de Takahara | rel=r_associated | relid=0 | w=44
- en:acatalasia --
r_associated #0: 42 / 0.857 ->
acatalasies
n1=en:acatalasia | n2=acatalasies | rel=r_associated | relid=0 | w=42
- en:acatalasia --
r_associated #0: 30 / 0.612 ->
acatalasémie de type japonais
n1=en:acatalasia | n2=acatalasémie de type japonais | rel=r_associated | relid=0 | w=30
- en:acatalasia --
r_associated #0: 30 / 0.612 ->
acatalasie
n1=en:acatalasia | n2=acatalasie | rel=r_associated | relid=0 | w=30
- en:acatalasia --
r_associated #0: 29 / 0.592 ->
acatalasémie de type suisse
n1=en:acatalasia | n2=acatalasémie de type suisse | rel=r_associated | relid=0 | w=29
- en:acatalasia --
r_associated #0: 29 / 0.592 ->
catalase
n1=en:acatalasia | n2=catalase | rel=r_associated | relid=0 | w=29
- en:acatalasia --
r_associated #0: 27 / 0.551 ->
déficience en catalase
n1=en:acatalasia | n2=déficience en catalase | rel=r_associated | relid=0 | w=27
- en:acatalasia --
r_associated #0: 27 / 0.551 ->
déficit en catalase
n1=en:acatalasia | n2=déficit en catalase | rel=r_associated | relid=0 | w=27
- en:acatalasia --
r_associated #0: 27 / 0.551 ->
maladie de takahara
n1=en:acatalasia | n2=maladie de takahara | rel=r_associated | relid=0 | w=27
- en:acatalasia --
r_associated #0: 26 / 0.531 ->
en:catalase deficiency
n1=en:acatalasia | n2=en:catalase deficiency | rel=r_associated | relid=0 | w=26
- en:acatalasia --
r_associated #0: 23 / 0.469 ->
en:acatalasemia japanese type
n1=en:acatalasia | n2=en:acatalasemia japanese type | rel=r_associated | relid=0 | w=23
- en:acatalasia --
r_associated #0: 23 / 0.469 ->
processus pathologique
n1=en:acatalasia | n2=processus pathologique | rel=r_associated | relid=0 | w=23
- en:acatalasia --
r_associated #0: 22 / 0.449 ->
acatalasique
n1=en:acatalasia | n2=acatalasique | rel=r_associated | relid=0 | w=22
- en:acatalasia --
r_associated #0: 22 / 0.449 ->
en:acatalasemia swiss type
n1=en:acatalasia | n2=en:acatalasemia swiss type | rel=r_associated | relid=0 | w=22
- en:acatalasia --
r_associated #0: 22 / 0.449 ->
en:hypocatalasemia
n1=en:acatalasia | n2=en:hypocatalasemia | rel=r_associated | relid=0 | w=22
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
coeur triatrial
n1=en:acatalasia | n2=coeur triatrial | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:acrodysostosis 1
n1=en:acatalasia | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:alders syndrome
n1=en:acatalasia | n2=en:alders syndrome | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:ataxia-telangiectasisa-like disorder 1
n1=en:acatalasia | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:carbonic anhydrase i deficiency
n1=en:acatalasia | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:cor triatriatum
n1=en:acatalasia | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:cortical dysplasia-focal epilepsy syndrome
n1=en:acatalasia | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia
n1=en:acatalasia | n2=en:dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:eiken type chondrodysplasia
n1=en:acatalasia | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:isolated alkyldihydroxyacetone phosphate synthase deficiency
n1=en:acatalasia | n2=en:isolated alkyldihydroxyacetone phosphate synthase deficiency | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:isolated dihydroxyacetone phosphate acyltransferase deficiency
n1=en:acatalasia | n2=en:isolated dihydroxyacetone phosphate acyltransferase deficiency | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:lethal neonatal rigidity and multifocal seizure syndrome
n1=en:acatalasia | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
n1=en:acatalasia | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:mental retardation, autosomal dominant 9
n1=en:acatalasia | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:mental retardation, autosomal recessive 34
n1=en:acatalasia | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:microcephaly and chorioretinopathy, autosomal recessive, type 1
n1=en:acatalasia | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:mitochondrial dna depletion syndrome 12
n1=en:acatalasia | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:mucolipidosis type iii gamma
n1=en:acatalasia | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:other group 2 peroxisomal disorders
n1=en:acatalasia | n2=en:other group 2 peroxisomal disorders | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:plasma kallikrein deficiency
n1=en:acatalasia | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 20 / 0.408 ->
en:tissue kallikrein deficiency
n1=en:acatalasia | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
- en:acatalasia --
r_associated #0: 15 / 0.306 ->
en:Takahara's disease
n1=en:acatalasia | n2=en:Takahara's disease | rel=r_associated | relid=0 | w=15
- en:acatalasia --
r_associated #0: 15 / 0.306 ->
Takahara (maladie de)
n1=en:acatalasia | n2=Takahara (maladie de) | rel=r_associated | relid=0 | w=15
| ≈ 38 relations entrantes
- maladie de takahara ---
r_associated #0: 48 -->
en:acatalasia
n1=maladie de takahara | n2=en:acatalasia | rel=r_associated | relid=0 | w=48
- maladie de Takahara ---
r_associated #0: 45 -->
en:acatalasia
n1=maladie de Takahara | n2=en:acatalasia | rel=r_associated | relid=0 | w=45
- acatalasémie ---
r_associated #0: 43 -->
en:acatalasia
n1=acatalasémie | n2=en:acatalasia | rel=r_associated | relid=0 | w=43
- en:Takahara's disease ---
r_associated #0: 42 -->
en:acatalasia
n1=en:Takahara's disease | n2=en:acatalasia | rel=r_associated | relid=0 | w=42
- en:carbonic anhydrase i deficiency ---
r_associated #0: 42 -->
en:acatalasia
n1=en:carbonic anhydrase i deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=42
- en:cortical dysplasia-focal epilepsy syndrome ---
r_associated #0: 41 -->
en:acatalasia
n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:acatalasia | rel=r_associated | relid=0 | w=41
- Takahara (maladie de) ---
r_associated #0: 40 -->
en:acatalasia
n1=Takahara (maladie de) | n2=en:acatalasia | rel=r_associated | relid=0 | w=40
- en:plasma kallikrein deficiency ---
r_associated #0: 40 -->
en:acatalasia
n1=en:plasma kallikrein deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=40
- en:acatalasemia ---
r_associated #0: 39 -->
en:acatalasia
n1=en:acatalasemia | n2=en:acatalasia | rel=r_associated | relid=0 | w=39
- en:other group 2 peroxisomal disorders ---
r_associated #0: 35 -->
en:acatalasia
n1=en:other group 2 peroxisomal disorders | n2=en:acatalasia | rel=r_associated | relid=0 | w=35
- acatalasies ---
r_associated #0: 34 -->
en:acatalasia
n1=acatalasies | n2=en:acatalasia | rel=r_associated | relid=0 | w=34
- en:lethal neonatal rigidity and multifocal seizure syndrome ---
r_associated #0: 34 -->
en:acatalasia
n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:acatalasia | rel=r_associated | relid=0 | w=34
- en:dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia ---
r_associated #0: 32 -->
en:acatalasia
n1=en:dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia | n2=en:acatalasia | rel=r_associated | relid=0 | w=32
- en:mucolipidosis type iii gamma ---
r_associated #0: 32 -->
en:acatalasia
n1=en:mucolipidosis type iii gamma | n2=en:acatalasia | rel=r_associated | relid=0 | w=32
- en:alders syndrome ---
r_associated #0: 31 -->
en:acatalasia
n1=en:alders syndrome | n2=en:acatalasia | rel=r_associated | relid=0 | w=31
- cœur triatrial ---
r_associated #0: 30 -->
en:acatalasia
n1=cœur triatrial | n2=en:acatalasia | rel=r_associated | relid=0 | w=30
- coeur triatrial ---
r_associated #0: 30 -->
en:acatalasia
n1=coeur triatrial | n2=en:acatalasia | rel=r_associated | relid=0 | w=30
- en:mental retardation, autosomal recessive 34 ---
r_associated #0: 29 -->
en:acatalasia
n1=en:mental retardation, autosomal recessive 34 | n2=en:acatalasia | rel=r_associated | relid=0 | w=29
- en:microcephaly and chorioretinopathy, autosomal recessive, type 1 ---
r_associated #0: 29 -->
en:acatalasia
n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:acatalasia | rel=r_associated | relid=0 | w=29
- en:mitochondrial dna depletion syndrome 12 ---
r_associated #0: 29 -->
en:acatalasia
n1=en:mitochondrial dna depletion syndrome 12 | n2=en:acatalasia | rel=r_associated | relid=0 | w=29
- en:tissue kallikrein deficiency ---
r_associated #0: 29 -->
en:acatalasia
n1=en:tissue kallikrein deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=29
- en:eiken type chondrodysplasia ---
r_associated #0: 28 -->
en:acatalasia
n1=en:eiken type chondrodysplasia | n2=en:acatalasia | rel=r_associated | relid=0 | w=28
- en:isolated alkyldihydroxyacetone phosphate synthase deficiency ---
r_associated #0: 28 -->
en:acatalasia
n1=en:isolated alkyldihydroxyacetone phosphate synthase deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=28
- en:isolated dihydroxyacetone phosphate acyltransferase deficiency ---
r_associated #0: 28 -->
en:acatalasia
n1=en:isolated dihydroxyacetone phosphate acyltransferase deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=28
- en:mental retardation, autosomal dominant 9 ---
r_associated #0: 28 -->
en:acatalasia
n1=en:mental retardation, autosomal dominant 9 | n2=en:acatalasia | rel=r_associated | relid=0 | w=28
- en:ataxia-telangiectasisa-like disorder 1 ---
r_associated #0: 27 -->
en:acatalasia
n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:acatalasia | rel=r_associated | relid=0 | w=27
- acatalasie ---
r_associated #0: 26 -->
en:acatalasia
n1=acatalasie | n2=en:acatalasia | rel=r_associated | relid=0 | w=26
- en:acrodysostosis 1 ---
r_associated #0: 26 -->
en:acatalasia
n1=en:acrodysostosis 1 | n2=en:acatalasia | rel=r_associated | relid=0 | w=26
- en:cor triatriatum ---
r_associated #0: 26 -->
en:acatalasia
n1=en:cor triatriatum | n2=en:acatalasia | rel=r_associated | relid=0 | w=26
- en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency ---
r_associated #0: 26 -->
en:acatalasia
n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=26
- acatalasémie de type japonais ---
r_associated #0: 21 -->
en:acatalasia
n1=acatalasémie de type japonais | n2=en:acatalasia | rel=r_associated | relid=0 | w=21
- acatalasémie de type suisse ---
r_associated #0: 21 -->
en:acatalasia
n1=acatalasémie de type suisse | n2=en:acatalasia | rel=r_associated | relid=0 | w=21
- déficience en catalase ---
r_associated #0: 21 -->
en:acatalasia
n1=déficience en catalase | n2=en:acatalasia | rel=r_associated | relid=0 | w=21
- déficit en catalase ---
r_associated #0: 21 -->
en:acatalasia
n1=déficit en catalase | n2=en:acatalasia | rel=r_associated | relid=0 | w=21
- catalase ---
r_associated #0: 20 -->
en:acatalasia
n1=catalase | n2=en:acatalasia | rel=r_associated | relid=0 | w=20
- en:catalase deficiency ---
r_associated #0: 20 -->
en:acatalasia
n1=en:catalase deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=20
- Catalase ---
r_associated #0: 10 -->
en:acatalasia
n1=Catalase | n2=en:acatalasia | rel=r_associated | relid=0 | w=10
- en:catalase ---
r_associated #0: 10 -->
en:acatalasia
n1=en:catalase | n2=en:acatalasia | rel=r_associated | relid=0 | w=10
|