'en:focal palmoplantar and gingival keratoderma'
(id=12928322 ; fe=en:focal palmoplantar and gingival keratoderma ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=482 creation date=2019-07-20 touchdate=2024-09-19 01:01:27.000) ≈ 14 relations sortantes
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 25 / 1 ->
en:focal
n1=en:focal palmoplantar and gingival keratoderma | n2=en:focal | rel=r_associated | relid=0 | w=25
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:chronic diarrhea with villous atrophy syndrome
n1=en:focal palmoplantar and gingival keratoderma | n2=en:chronic diarrhea with villous atrophy syndrome | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:congenital laryngeal cyst
n1=en:focal palmoplantar and gingival keratoderma | n2=en:congenital laryngeal cyst | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:corneal dystrophy, subepithelial mucinous
n1=en:focal palmoplantar and gingival keratoderma | n2=en:corneal dystrophy, subepithelial mucinous | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:epiphyseal dysplasia, multiple, 2
n1=en:focal palmoplantar and gingival keratoderma | n2=en:epiphyseal dysplasia, multiple, 2 | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:ferro-cerebro-cutaneous syndrome
n1=en:focal palmoplantar and gingival keratoderma | n2=en:ferro-cerebro-cutaneous syndrome | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:genetic disorder of skin pigmentation
n1=en:focal palmoplantar and gingival keratoderma | n2=en:genetic disorder of skin pigmentation | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
n1=en:focal palmoplantar and gingival keratoderma | n2=en:hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome
n1=en:focal palmoplantar and gingival keratoderma | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:non-androgenic hypertrichosis with genetic disease
n1=en:focal palmoplantar and gingival keratoderma | n2=en:non-androgenic hypertrichosis with genetic disease | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:pigmented paravenous chorioretinal atrophy
n1=en:focal palmoplantar and gingival keratoderma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:polydactyly, preaxial ii (disorder)
n1=en:focal palmoplantar and gingival keratoderma | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome
n1=en:focal palmoplantar and gingival keratoderma | n2=en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome | rel=r_associated | relid=0 | w=20
- en:focal palmoplantar and gingival keratoderma --
r_associated #0: 20 / 0.8 ->
rétinite pigmentaire paraveineuse
n1=en:focal palmoplantar and gingival keratoderma | n2=rétinite pigmentaire paraveineuse | rel=r_associated | relid=0 | w=20
| ≈ 14 relations entrantes
- rétinite pigmentaire paraveineuse ---
r_associated #0: 45 -->
en:focal palmoplantar and gingival keratoderma
n1=rétinite pigmentaire paraveineuse | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=45
- en:pigmented paravenous chorioretinal atrophy ---
r_associated #0: 41 -->
en:focal palmoplantar and gingival keratoderma
n1=en:pigmented paravenous chorioretinal atrophy | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=41
- en:ferro-cerebro-cutaneous syndrome ---
r_associated #0: 38 -->
en:focal palmoplantar and gingival keratoderma
n1=en:ferro-cerebro-cutaneous syndrome | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=38
- en:corneal dystrophy, subepithelial mucinous ---
r_associated #0: 35 -->
en:focal palmoplantar and gingival keratoderma
n1=en:corneal dystrophy, subepithelial mucinous | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=35
- en:epiphyseal dysplasia, multiple, 2 ---
r_associated #0: 35 -->
en:focal palmoplantar and gingival keratoderma
n1=en:epiphyseal dysplasia, multiple, 2 | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=35
- en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome ---
r_associated #0: 35 -->
en:focal palmoplantar and gingival keratoderma
n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=35
- en:congenital laryngeal cyst ---
r_associated #0: 32 -->
en:focal palmoplantar and gingival keratoderma
n1=en:congenital laryngeal cyst | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=32
- en:non-androgenic hypertrichosis with genetic disease ---
r_associated #0: 32 -->
en:focal palmoplantar and gingival keratoderma
n1=en:non-androgenic hypertrichosis with genetic disease | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=32
- en:genetic disorder of skin pigmentation ---
r_associated #0: 31 -->
en:focal palmoplantar and gingival keratoderma
n1=en:genetic disorder of skin pigmentation | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=31
- en:polydactyly, preaxial ii (disorder) ---
r_associated #0: 30 -->
en:focal palmoplantar and gingival keratoderma
n1=en:polydactyly, preaxial ii (disorder) | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=30
- en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome ---
r_associated #0: 29 -->
en:focal palmoplantar and gingival keratoderma
n1=en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=29
- en:chronic diarrhea with villous atrophy syndrome ---
r_associated #0: 27 -->
en:focal palmoplantar and gingival keratoderma
n1=en:chronic diarrhea with villous atrophy syndrome | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=27
- en:hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome ---
r_associated #0: 27 -->
en:focal palmoplantar and gingival keratoderma
n1=en:hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=27
- rétinite pigmentaire liée à la périphérine (pro219leu) ---
r_associated #0: 10 -->
en:focal palmoplantar and gingival keratoderma
n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=10
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