'en:neurofibromatoses'
(id=8989802 ; fe=en:neurofibromatoses ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=3288 creation date=2017-10-06 touchdate=2025-12-02 01:09:46.000) ≈ 84 relations sortantes
- en:neurofibromatoses --
r_associated #0: 100 / 1 ->
neurofibromatose de type III
n1=en:neurofibromatoses | n2=neurofibromatose de type III | rel=r_associated | relid=0 | w=100
- en:neurofibromatoses --
r_associated #0: 98 / 0.98 ->
neurofibromatose de type 3
n1=en:neurofibromatoses | n2=neurofibromatose de type 3 | rel=r_associated | relid=0 | w=98
- en:neurofibromatoses --
r_associated #0: 97 / 0.97 ->
en:neurofibromatosis
n1=en:neurofibromatoses | n2=en:neurofibromatosis | rel=r_associated | relid=0 | w=97
- en:neurofibromatoses --
r_associated #0: 97 / 0.97 ->
en:neurofibromatosis 3s
n1=en:neurofibromatoses | n2=en:neurofibromatosis 3s | rel=r_associated | relid=0 | w=97
- en:neurofibromatoses --
r_associated #0: 95 / 0.95 ->
neurofibromatose multiple
n1=en:neurofibromatoses | n2=neurofibromatose multiple | rel=r_associated | relid=0 | w=95
- en:neurofibromatoses --
r_associated #0: 62 / 0.62 ->
problème de différenciation du tissu ectodermique chez l'embryon
n1=en:neurofibromatoses | n2=problème de différenciation du tissu ectodermique chez l'embryon | rel=r_associated | relid=0 | w=62
- en:neurofibromatoses --
r_associated #0: 56 / 0.56 ->
neurofibromatose, sai
n1=en:neurofibromatoses | n2=neurofibromatose, sai | rel=r_associated | relid=0 | w=56
- en:neurofibromatoses --
r_associated #0: 53 / 0.53 ->
maladie de von recklinghausen (à l'exception de la maladie osseuse)
n1=en:neurofibromatoses | n2=maladie de von recklinghausen (à l'exception de la maladie osseuse) | rel=r_associated | relid=0 | w=53
- en:neurofibromatoses --
r_associated #0: 52 / 0.52 ->
syndrome de neurofibromatose
n1=en:neurofibromatoses | n2=syndrome de neurofibromatose | rel=r_associated | relid=0 | w=52
- en:neurofibromatoses --
r_associated #0: 51 / 0.51 ->
neurofibromatose clinique
n1=en:neurofibromatoses | n2=neurofibromatose clinique | rel=r_associated | relid=0 | w=51
- en:neurofibromatoses --
r_associated #0: 34 / 0.34 ->
neurofibromes multiples
n1=en:neurofibromatoses | n2=neurofibromes multiples | rel=r_associated | relid=0 | w=34
- en:neurofibromatoses --
r_associated #0: 34 / 0.34 ->
processus pathologique
n1=en:neurofibromatoses | n2=processus pathologique | rel=r_associated | relid=0 | w=34
- en:neurofibromatoses --
r_associated #0: 31 / 0.31 ->
neurofibromatose
n1=en:neurofibromatoses | n2=neurofibromatose | rel=r_associated | relid=0 | w=31
- en:neurofibromatoses --
r_associated #0: 28 / 0.28 ->
neurofibromatoses
n1=en:neurofibromatoses | n2=neurofibromatoses | rel=r_associated | relid=0 | w=28
- en:neurofibromatoses --
r_associated #0: 28 / 0.28 ->
non précisée, neurofibromatose
n1=en:neurofibromatoses | n2=non précisée, neurofibromatose | rel=r_associated | relid=0 | w=28
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:absence of fingerprints with congenital milia syndrome
n1=en:neurofibromatoses | n2=en:absence of fingerprints with congenital milia syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:acro-dermato-ungual-lacrimal-tooth syndrome
n1=en:neurofibromatoses | n2=en:acro-dermato-ungual-lacrimal-tooth syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges
n1=en:neurofibromatoses | n2=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:aphalangy and syndactyly with microcephaly syndrome
n1=en:neurofibromatoses | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:arterial dissection and lentiginosis syndrome
n1=en:neurofibromatoses | n2=en:arterial dissection and lentiginosis syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:autosomal dominant focal dystonia dyt25 type
n1=en:neurofibromatoses | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:autosomal dominant palmoplantar keratoderma and congenital alopecia
n1=en:neurofibromatoses | n2=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:bamforth syndrome
n1=en:neurofibromatoses | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:basal epidermolysis bullosa simplex
n1=en:neurofibromatoses | n2=en:basal epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:blood vessel neoplasm, uncertain whether benign or malignant
n1=en:neurofibromatoses | n2=en:blood vessel neoplasm, uncertain whether benign or malignant | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:brain calcification rajab type
n1=en:neurofibromatoses | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:cervical hypertrichosis and peripheral neuropathy syndrome
n1=en:neurofibromatoses | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:cns-excluded nervous system neoplasm and disorder
n1=en:neurofibromatoses | n2=en:cns-excluded nervous system neoplasm and disorder | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:constitutional mismatch repair deficiency syndrome
n1=en:neurofibromatoses | n2=en:constitutional mismatch repair deficiency syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:cutaneous photosensitivity and lethal colitis syndrome
n1=en:neurofibromatoses | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:diffuse palmoplantar keratoderma and acrocyanosis syndrome
n1=en:neurofibromatoses | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:ectodermal dysplasia with blindness syndrome
n1=en:neurofibromatoses | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:fibromatous neoplasm of borderline malignancy
n1=en:neurofibromatoses | n2=en:fibromatous neoplasm of borderline malignancy | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:generalized peeling skin syndrome
n1=en:neurofibromatoses | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:genetic disorder of skin pigmentation
n1=en:neurofibromatoses | n2=en:genetic disorder of skin pigmentation | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:glioma, uncertain whether benign or malignant
n1=en:neurofibromatoses | n2=en:glioma, uncertain whether benign or malignant | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:halal syndrome
n1=en:neurofibromatoses | n2=en:halal syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:hall riggs syndrome
n1=en:neurofibromatoses | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:hypertrichosis and acromegaloid facial appearance syndrome
n1=en:neurofibromatoses | n2=en:hypertrichosis and acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:hypohidrosis due to genetic abnormality of eccrine gland structure and function
n1=en:neurofibromatoses | n2=en:hypohidrosis due to genetic abnormality of eccrine gland structure and function | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:insulin growth factor i deficiency
n1=en:neurofibromatoses | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:juvenile amyotrophic lateral sclerosis
n1=en:neurofibromatoses | n2=en:juvenile amyotrophic lateral sclerosis | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:late-onset junctional epidermolysis bullosa
n1=en:neurofibromatoses | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome
n1=en:neurofibromatoses | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:lissencephaly type 3 familial fetal akinesia sequence syndrome
n1=en:neurofibromatoses | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:microcephaly albinism digital anomalies syndrome
n1=en:neurofibromatoses | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:micronodular thymoma with lymphoid stroma
n1=en:neurofibromatoses | n2=en:micronodular thymoma with lymphoid stroma | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:moyamoya disease with early onset achalasia
n1=en:neurofibromatoses | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:multiple fibromatosis
n1=en:neurofibromatoses | n2=en:multiple fibromatosis | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:multiple neuroma
n1=en:neurofibromatoses | n2=en:multiple neuroma | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:myxoid neurofibroma
n1=en:neurofibromatoses | n2=en:myxoid neurofibroma | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:nci ctep sdc neurofibromatosis sub-category terminology
n1=en:neurofibromatoses | n2=en:nci ctep sdc neurofibromatosis sub-category terminology | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:neurofibromatosis type III
n1=en:neurofibromatoses | n2=en:neurofibromatosis type III | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome
n1=en:neurofibromatoses | n2=en:neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:neurofibromatosis, familial intestinal
n1=en:neurofibromatoses | n2=en:neurofibromatosis, familial intestinal | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:neurofibromatosis, familial spinal
n1=en:neurofibromatoses | n2=en:neurofibromatosis, familial spinal | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:neurofibromatosis, type 3, mixed central and peripheral
n1=en:neurofibromatoses | n2=en:neurofibromatosis, type 3, mixed central and peripheral | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:neurofibromatosis, type 4, of riccardi
n1=en:neurofibromatoses | n2=en:neurofibromatosis, type 4, of riccardi | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:neuromatosis
n1=en:neurofibromatoses | n2=en:neuromatosis | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:nf1 microdeletion syndrome
n1=en:neurofibromatoses | n2=en:nf1 microdeletion syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:nf1 microduplication syndrome
n1=en:neurofibromatoses | n2=en:nf1 microduplication syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:non-androgenic hypertrichosis with genetic disease
n1=en:neurofibromatoses | n2=en:non-androgenic hypertrichosis with genetic disease | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:painful orbital and systemic neurofibromas-marfanoid habitus syndrome
n1=en:neurofibromatoses | n2=en:painful orbital and systemic neurofibromas-marfanoid habitus syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome
n1=en:neurofibromatoses | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:pili torti onychodysplasia syndrome
n1=en:neurofibromatoses | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
n1=en:neurofibromatoses | n2=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:pterygium colli mental retardation digital anomalies
n1=en:neurofibromatoses | n2=en:pterygium colli mental retardation digital anomalies | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:ras-associated autoimmune leukoproliferative disorder
n1=en:neurofibromatoses | n2=en:ras-associated autoimmune leukoproliferative disorder | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:scholte syndrome
n1=en:neurofibromatoses | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:von Recklinghausen's disease
n1=en:neurofibromatoses | n2=en:von Recklinghausen's disease | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
n1=en:neurofibromatoses | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:x-linked intellectual disability with ataxia and apraxia syndrome
n1=en:neurofibromatoses | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
n1=en:neurofibromatoses | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:x-linked recessive hypophosphatemic rickets
n1=en:neurofibromatoses | n2=en:x-linked recessive hypophosphatemic rickets | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
en:yemenite deaf-blind hypopigmentation syndrome
n1=en:neurofibromatoses | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
neurofibromatose de recklinghausen
n1=en:neurofibromatoses | n2=neurofibromatose de recklinghausen | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
neurofibromatose de Recklinghausen
n1=en:neurofibromatoses | n2=neurofibromatose de Recklinghausen | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
neurofibromatose de type périphérique
n1=en:neurofibromatoses | n2=neurofibromatose de type périphérique | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
neurofibromatose de type VI
n1=en:neurofibromatoses | n2=neurofibromatose de type VI | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
NF-3
n1=en:neurofibromatoses | n2=NF-3 | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 20 / 0.2 ->
Recklinghausen (neurofibromatose de)
n1=en:neurofibromatoses | n2=Recklinghausen (neurofibromatose de) | rel=r_associated | relid=0 | w=20
- en:neurofibromatoses --
r_associated #0: 8 / 0.08 ->
problème
n1=en:neurofibromatoses | n2=problème | rel=r_associated | relid=0 | w=8
- en:neurofibromatoses --
r_associated #0: 5 / 0.05 ->
maladie de von Recklinghausen
n1=en:neurofibromatoses | n2=maladie de von Recklinghausen | rel=r_associated | relid=0 | w=5
- en:neurofibromatoses --
r_associated #0: 5 / 0.05 ->
Recklinghausen (maladie de von)
n1=en:neurofibromatoses | n2=Recklinghausen (maladie de von) | rel=r_associated | relid=0 | w=5
| ≈ 96 relations entrantes
- Recklinghausen (neurofibromatose de) ---
r_associated #0: 51 -->
en:neurofibromatoses
n1=Recklinghausen (neurofibromatose de) | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=51
- neurofibromatose ---
r_associated #0: 51 -->
en:neurofibromatoses
n1=neurofibromatose | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=51
- en:neurofibromatosis ---
r_associated #0: 50 -->
en:neurofibromatoses
n1=en:neurofibromatosis | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=50
- en:aphalangy and syndactyly with microcephaly syndrome ---
r_associated #0: 42 -->
en:neurofibromatoses
n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=42
- en:von Recklinghausen's disease ---
r_associated #0: 42 -->
en:neurofibromatoses
n1=en:von Recklinghausen's disease | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=42
- neurofibromatose de Recklinghausen ---
r_associated #0: 40 -->
en:neurofibromatoses
n1=neurofibromatose de Recklinghausen | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=40
- neurofibromatose de recklinghausen ---
r_associated #0: 40 -->
en:neurofibromatoses
n1=neurofibromatose de recklinghausen | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=40
- neurofibromatose de type périphérique ---
r_associated #0: 40 -->
en:neurofibromatoses
n1=neurofibromatose de type périphérique | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=40
- en:cutaneous photosensitivity and lethal colitis syndrome ---
r_associated #0: 39 -->
en:neurofibromatoses
n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=39
- en:yemenite deaf-blind hypopigmentation syndrome ---
r_associated #0: 38 -->
en:neurofibromatoses
n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=38
- en:hypertrichosis and acromegaloid facial appearance syndrome ---
r_associated #0: 37 -->
en:neurofibromatoses
n1=en:hypertrichosis and acromegaloid facial appearance syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=37
- en:non-androgenic hypertrichosis with genetic disease ---
r_associated #0: 37 -->
en:neurofibromatoses
n1=en:non-androgenic hypertrichosis with genetic disease | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=37
- neurofibromatose de type III ---
r_associated #0: 36 -->
en:neurofibromatoses
n1=neurofibromatose de type III | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=36
- neurofibromatose de type VI ---
r_associated #0: 36 -->
en:neurofibromatoses
n1=neurofibromatose de type VI | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=36
- en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges ---
r_associated #0: 35 -->
en:neurofibromatoses
n1=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=35
- en:arterial dissection and lentiginosis syndrome ---
r_associated #0: 35 -->
en:neurofibromatoses
n1=en:arterial dissection and lentiginosis syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=35
- en:basal epidermolysis bullosa simplex ---
r_associated #0: 35 -->
en:neurofibromatoses
n1=en:basal epidermolysis bullosa simplex | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=35
- en:cervical hypertrichosis and peripheral neuropathy syndrome ---
r_associated #0: 35 -->
en:neurofibromatoses
n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=35
- en:lissencephaly type 3 familial fetal akinesia sequence syndrome ---
r_associated #0: 35 -->
en:neurofibromatoses
n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=35
- en:multiple neuroma ---
r_associated #0: 35 -->
en:neurofibromatoses
n1=en:multiple neuroma | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=35
- neurofibromatose, sai ---
r_associated #0: 35 -->
en:neurofibromatoses
n1=neurofibromatose, sai | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=35
- en:blood vessel neoplasm, uncertain whether benign or malignant ---
r_associated #0: 34 -->
en:neurofibromatoses
n1=en:blood vessel neoplasm, uncertain whether benign or malignant | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=34
- en:hall riggs syndrome ---
r_associated #0: 34 -->
en:neurofibromatoses
n1=en:hall riggs syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=34
- en:neurofibromatosis, familial intestinal ---
r_associated #0: 34 -->
en:neurofibromatoses
n1=en:neurofibromatosis, familial intestinal | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=34
- en:neurofibromatosis, type 3, mixed central and peripheral ---
r_associated #0: 34 -->
en:neurofibromatoses
n1=en:neurofibromatosis, type 3, mixed central and peripheral | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=34
- en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome ---
r_associated #0: 34 -->
en:neurofibromatoses
n1=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=34
- en:neurofibromatosis type III ---
r_associated #0: 33 -->
en:neurofibromatoses
n1=en:neurofibromatosis type III | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=33
- en:bamforth syndrome ---
r_associated #0: 32 -->
en:neurofibromatoses
n1=en:bamforth syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=32
- en:brain calcification rajab type ---
r_associated #0: 32 -->
en:neurofibromatoses
n1=en:brain calcification rajab type | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=32
- en:constitutional mismatch repair deficiency syndrome ---
r_associated #0: 32 -->
en:neurofibromatoses
n1=en:constitutional mismatch repair deficiency syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=32
- en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome ---
r_associated #0: 32 -->
en:neurofibromatoses
n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=32
- en:micronodular thymoma with lymphoid stroma ---
r_associated #0: 32 -->
en:neurofibromatoses
n1=en:micronodular thymoma with lymphoid stroma | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=32
- en:neurofibromatosis, familial spinal ---
r_associated #0: 32 -->
en:neurofibromatoses
n1=en:neurofibromatosis, familial spinal | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=32
- en:pterygium colli mental retardation digital anomalies ---
r_associated #0: 32 -->
en:neurofibromatoses
n1=en:pterygium colli mental retardation digital anomalies | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=32
- en:absence of fingerprints with congenital milia syndrome ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:absence of fingerprints with congenital milia syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:cns-excluded nervous system neoplasm and disorder ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:cns-excluded nervous system neoplasm and disorder | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:hypohidrosis due to genetic abnormality of eccrine gland structure and function ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:hypohidrosis due to genetic abnormality of eccrine gland structure and function | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:late-onset junctional epidermolysis bullosa ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:late-onset junctional epidermolysis bullosa | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:nci ctep sdc neurofibromatosis sub-category terminology ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:nci ctep sdc neurofibromatosis sub-category terminology | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:neuromatosis ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:neuromatosis | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:pili torti onychodysplasia syndrome ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:pili torti onychodysplasia syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:scholte syndrome ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:scholte syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability with acromegaly and hyperactivity syndrome ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome ---
r_associated #0: 31 -->
en:neurofibromatoses
n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=31
- en:autosomal dominant focal dystonia dyt25 type ---
r_associated #0: 30 -->
en:neurofibromatoses
n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=30
- en:diffuse palmoplantar keratoderma and acrocyanosis syndrome ---
r_associated #0: 30 -->
en:neurofibromatoses
n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=30
- en:neurofibromatosis 3s ---
r_associated #0: 30 -->
en:neurofibromatoses
n1=en:neurofibromatosis 3s | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=30
- en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome ---
r_associated #0: 30 -->
en:neurofibromatoses
n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=30
- en:ras-associated autoimmune leukoproliferative disorder ---
r_associated #0: 30 -->
en:neurofibromatoses
n1=en:ras-associated autoimmune leukoproliferative disorder | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=30
- en:generalized peeling skin syndrome ---
r_associated #0: 29 -->
en:neurofibromatoses
n1=en:generalized peeling skin syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=29
- en:halal syndrome ---
r_associated #0: 29 -->
en:neurofibromatoses
n1=en:halal syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=29
- en:juvenile amyotrophic lateral sclerosis ---
r_associated #0: 29 -->
en:neurofibromatoses
n1=en:juvenile amyotrophic lateral sclerosis | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=29
- en:myxoid neurofibroma ---
r_associated #0: 29 -->
en:neurofibromatoses
n1=en:myxoid neurofibroma | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=29
- neurofibromatose de type 3 ---
r_associated #0: 29 -->
en:neurofibromatoses
n1=neurofibromatose de type 3 | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=29
- NF-3 ---
r_associated #0: 28 -->
en:neurofibromatoses
n1=NF-3 | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=28
- en:autosomal dominant palmoplantar keratoderma and congenital alopecia ---
r_associated #0: 28 -->
en:neurofibromatoses
n1=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=28
- en:genetic disorder of skin pigmentation ---
r_associated #0: 28 -->
en:neurofibromatoses
n1=en:genetic disorder of skin pigmentation | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=28
- en:insulin growth factor i deficiency ---
r_associated #0: 28 -->
en:neurofibromatoses
n1=en:insulin growth factor i deficiency | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=28
- en:microcephaly albinism digital anomalies syndrome ---
r_associated #0: 28 -->
en:neurofibromatoses
n1=en:microcephaly albinism digital anomalies syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=28
- en:neurofibromatosis, type 4, of riccardi ---
r_associated #0: 28 -->
en:neurofibromatoses
n1=en:neurofibromatosis, type 4, of riccardi | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=28
- en:nf1 microduplication syndrome ---
r_associated #0: 28 -->
en:neurofibromatoses
n1=en:nf1 microduplication syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability with ataxia and apraxia syndrome ---
r_associated #0: 28 -->
en:neurofibromatoses
n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=28
- en:acro-dermato-ungual-lacrimal-tooth syndrome ---
r_associated #0: 27 -->
en:neurofibromatoses
n1=en:acro-dermato-ungual-lacrimal-tooth syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=27
- en:ectodermal dysplasia with blindness syndrome ---
r_associated #0: 27 -->
en:neurofibromatoses
n1=en:ectodermal dysplasia with blindness syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=27
- en:multiple fibromatosis ---
r_associated #0: 27 -->
en:neurofibromatoses
n1=en:multiple fibromatosis | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=27
- en:nf1 microdeletion syndrome ---
r_associated #0: 27 -->
en:neurofibromatoses
n1=en:nf1 microdeletion syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=27
- en:painful orbital and systemic neurofibromas-marfanoid habitus syndrome ---
r_associated #0: 27 -->
en:neurofibromatoses
n1=en:painful orbital and systemic neurofibromas-marfanoid habitus syndrome | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=27
- syndrome de neurofibromatose ---
r_associated #0: 27 -->
en:neurofibromatoses
n1=syndrome de neurofibromatose | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=27
- en:fibromatous neoplasm of borderline malignancy ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=en:fibromatous neoplasm of borderline malignancy | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- en:glioma, uncertain whether benign or malignant ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=en:glioma, uncertain whether benign or malignant | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- en:moyamoya disease with early onset achalasia ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=en:moyamoya disease with early onset achalasia | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- en:x-linked recessive hypophosphatemic rickets ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=en:x-linked recessive hypophosphatemic rickets | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- maladie de von recklinghausen (à l'exception de la maladie osseuse) ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=maladie de von recklinghausen (à l'exception de la maladie osseuse) | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- neurofibromatose clinique ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=neurofibromatose clinique | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- neurofibromatose multiple ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=neurofibromatose multiple | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- neurofibromatose non précisée ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=neurofibromatose non précisée | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- neurofibromes multiples ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=neurofibromes multiples | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- non précisée, neurofibromatose ---
r_associated #0: 26 -->
en:neurofibromatoses
n1=non précisée, neurofibromatose | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=26
- maladie de Recklinghausen ---
r_associated #0: 25 -->
en:neurofibromatoses
n1=maladie de Recklinghausen | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=25
- maladie de von Recklinghausen ---
r_associated #0: 24 -->
en:neurofibromatoses
n1=maladie de von Recklinghausen | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=24
- Recklinghausen (maladie de von) ---
r_associated #0: 23 -->
en:neurofibromatoses
n1=Recklinghausen (maladie de von) | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=23
- neurofibromatose de type 1 ---
r_associated #0: 22 -->
en:neurofibromatoses
n1=neurofibromatose de type 1 | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=22
- neurofibromatoses ---
r_associated #0: 21 -->
en:neurofibromatoses
n1=neurofibromatoses | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=21
- problème de différenciation du tissu ectodermique chez l'embryon ---
r_associated #0: 20 -->
en:neurofibromatoses
n1=problème de différenciation du tissu ectodermique chez l'embryon | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=20
- processus pathologique ---
r_associated #0: 20 -->
en:neurofibromatoses
n1=processus pathologique | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=20
- maladie clinique de recklinghausen ---
r_associated #0: 15 -->
en:neurofibromatoses
n1=maladie clinique de recklinghausen | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=15
- Neurofibromatose ---
r_associated #0: 10 -->
en:neurofibromatoses
n1=Neurofibromatose | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=10
- Syndrome de Neurofibromatose ---
r_associated #0: 10 -->
en:neurofibromatoses
n1=Syndrome de Neurofibromatose | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=10
- absence d'empreintes digitales avec syndrome de milia congénital ---
r_associated #0: 10 -->
en:neurofibromatoses
n1=absence d'empreintes digitales avec syndrome de milia congénital | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=10
- en:Recklinghausen's disease ---
r_associated #0: 10 -->
en:neurofibromatoses
n1=en:Recklinghausen's disease | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=10
- en:type I ---
r_associated #0: 10 -->
en:neurofibromatoses
n1=en:type I | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=10
- en:type VI ---
r_associated #0: 10 -->
en:neurofibromatoses
n1=en:type VI | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=10
- en:von recklinghausen's disease ---
r_associated #0: 10 -->
en:neurofibromatoses
n1=en:von recklinghausen's disease | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=10
- reclassement professionnel ---
r_associated #0: 10 -->
en:neurofibromatoses
n1=reclassement professionnel | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=10
- syndrome de Neurofibromatose ---
r_associated #0: 10 -->
en:neurofibromatoses
n1=syndrome de Neurofibromatose | n2=en:neurofibromatoses | rel=r_associated | relid=0 | w=10
|