Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital anomaly of fourth branchial cleft |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Congenital fistula of commissure of lips |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Non-syndromic metopic craniosynostosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Non-syndromic metopic craniosynostosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Isolated osteopoikilosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
46,XY disorder of sex development due to isolated 17,20-lyase deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital isolated adrenocorticotropic hormone deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital isolated adrenocorticotropic hormone deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Autosomal dominant generalized dystrophic epidermolysis bullosa (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital anomaly of left lower limb |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital anomaly of right lower limb (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Cardiac anomaly and heterotaxy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Deafness, enamel hypoplasia, nail defect syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
MYH9 related disease |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Congenital malformation of blood vessel of bilateral orbits proper (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Incomplete cleft lip (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Meningoencephalocele of orbit (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Meningoencephalocele of orbit (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Meningoencephalocele of orbit (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Meningoencephalocele of orbit (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
Complete cleft lip (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital meningocele of orbit (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital meningocele of orbit (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Syndromic nanophthalmos due to Kenny-Caffey syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Isolated agenesis of cerebellar vermis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Rathke's pouch cyst (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Limb girdle muscular dystrophy due to POMK deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Osteofibrous dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
14q32 duplication syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
14q32 duplication syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
46,XX ovotesticular disorder of sex development (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Ovotesticular disorder of sex development |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital azygos continuation of inferior vena cava (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital straddling and overriding tricuspid valve (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital cochleovestibular malformation |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital vascular malformation of orbital region (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Persistent congenital anteversion of femur (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
Encephalopathy due to mitochondrial and peroxisomal fission defect (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Kerasin thesaurismosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Distal muscular dystrophy with juvenile onset |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Carpenter's syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Congenital iodine deficiency syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Supernumerary permanent tooth |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Supernumerary tooth identifiable by tooth number |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Supernumerary tooth unidentifiable by tooth number |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Erupted mesiodens |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Inverted mesiodens |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Multiple supernumerary teeth unrelated to systemic condition |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Multiple supernumerary teeth related to systemic condition |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
encéphalopathie spongiforme |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Earpit syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Lymphatic malformation |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Conical supernumerary tooth |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Tuberculate supernumerary tooth |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Lip pits |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Commissural lip pits |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Midline sinus of the upper lip |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Hypothyroidism due to iodide organification defect |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Thyroid hormone resistance syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Generalized thyroid hormone resistance |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Generalised essential telangiectasia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Simple lymphangioma |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Lymphangioma circumscriptum |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Diffuse lymphangioma |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Lymphangiectases |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Systemic lymphangiomatosis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Acquired lymphangioma |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Acantholytic dyskeratotic epidermal naevus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Nevus striatus symmetricus of thumbs |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Epidermal naevus syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Genitoperineal raphe cyst |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Lumpy scalp syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
X-linked muscular dystrophy with limb girdle distribution |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
X-linked muscular dystrophy with abnormal dystrophin |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Intermediate X-linked muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Manifesting female carrier of X-linked muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
X-linked limb girdle muscular dystrophy with normal dystrophin |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Ji muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Hereditary myopathy limited to females |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Severe autosomal recessive muscular dystrophy of childhood - North African type |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Autosomal recessive muscular dystrophy with gene located at 15q |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Reunion-Indiana Amish type muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Congenital muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Western type of congenital muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Congenital muscular dystrophy with arthrogryposis multiplex congenita |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Ullrich congenital muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Eichsfeld type congenital muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Hutterite type of muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Adult onset autosomal recessive muscular dystrophy with normal dystrophin |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Autosomal dominant muscular dystrophy with limb girdle distribution |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Autosomal dominant muscular dystrophy with gene located at 5q31 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Late onset proximal muscular dystrophy with dysarthria |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
X-linked muscular dystrophy not predominantly limb girdle |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Benign scapuloperoneal muscular dystrophy with cardiomyopathy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Autosomal recessive muscular dystrophy not predominantly limb girdle |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Scapulohumeral muscular dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|