Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Charcot-Marie-Tooth disease type 4H (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Charcot-Marie-Tooth disease type 4B1 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Charcot-Marie-Tooth disease type 4J (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Autosomal dominant spastic paraplegia type 4 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal dominant spastic paraplegia type 10 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal dominant spastic paraplegia type 6 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
paraplégie spastique autosomique dominante type 31 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Bipartite talus (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Cleft palate, large ears, small head syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Chondroectodermal dysplasia with night blindness syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
Charcot-Marie-Tooth disease type 4E (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Combined pancreatic lipase and colipase deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Conductive deafness, ptosis, skeletal anomalies syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Congenital ankylosis of temporomandibular joint (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
anesthésie congénitale du nerf trijumeau |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Distal trisomy 2q |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Distal trisomy 4q (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
trisomie distale 5q |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Distal trisomy 6q |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Distal trisomy 7p syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Distal trisomy 8q |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Facial dysmorphism, cleft palate, loose skin syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Adrenomyodystrophy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
syndrome d'ataxie cérébelleuse autosomique récessive-signes pyramidaux-nystagmus-apraxie oculomotrice |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital muscular dystrophy with hyperlaxity (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Congenital myopathy with myasthenic-like onset (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital patent ductus arteriosus aneurysm |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Isolated congenital syngnathia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Connective tissue disorder due to lysyl hydroxylase-3 deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Craniofaciofrontodigital syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Charcot-Marie-Tooth disease type 4B3 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
syndrome d'akinésie foetale-hémorragies cérébrales et rétiniennes |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
X-linked Charcot-Marie-Tooth disease type 6 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Spectrin-associated autosomal recessive cerebellar ataxia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Cerebrofacioarticular syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Dentigerous cyst |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Cleft cartilaginous centrum of cervical vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Cleft cartilaginous centrum of lumbar vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Cleft cartilaginous centrum of sacral vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Cleft cartilaginous centrum of thoracic vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bipartite ossification of centrum of caudal vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bipartite ossification of centrum of cervical vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bipartite ossification of interparietal bone |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bipartite ossification of centrum of lumbar vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bipartite ossification of centrum of sacral vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bipartite ossification of sternebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bipartite ossification of supraoccipital bone |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bipartite ossification of centrum of thoracic vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Congenital cleft of thymus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bilateral acheiria |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Neurofibromatosis type 2 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bilateral congenital absence of feet |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Bilateral crossbite |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Buccal crossbite |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Congenital bowing of tibia and/or fibula (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
X-linked hereditary motor and sensory neuropathy |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
X-linked hereditary spastic paraplegia (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
Autosomal recessive spastic paraplegia type 48 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Familial progressive hyper and hypopigmentation |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 5A |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
paraplégie spastique autosomique type 30 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
X-linked Charcot-Marie-Tooth disease type 4 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Ichthyosis prematurity syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Carcinoma in situ of ectopic female breast tissue |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
carcinome in situ du tissu mammaire ectopique chez l'homme |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
forme létale du syndrome des ptérygiums multiples (trouble) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
forme létale du syndrome des ptérygiums multiples (trouble) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
forme létale du syndrome des ptérygiums multiples (trouble) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
Autosomal recessive spastic paraplegia type 11 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 39 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal dominant spastic paraplegia type 36 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 44 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 46 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 53 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 54 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 55 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
paraplégie spastique autosomique récessive type 57 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 32 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 26 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 23 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 64 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 63 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 61 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Spastic paraplegia with Paget disease of bone syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
paraplégie spastique autosomique récessive type 18 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal recessive spastic paraplegia type 25 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Autosomal dominant spastic paraplegia type 29 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Spastic paraplegia, facial cutaneous lesion syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
syndrome du chromosome 15 en anneau |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Ring chromosome 16 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Ring chromosome Y syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
X-linked Charcot-Marie-Tooth disease type 1 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
X-linked Charcot-Marie-Tooth disease type 2 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
X-linked Charcot-Marie-Tooth disease type 3 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
X-linked Charcot-Marie-Tooth disease type 5 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
X-linked lethal multiple pterygium syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |