| 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 |
|