| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Sphingolipid activator protein 1 deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Chronic gouty arthritis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Complete trisomy 8 syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Histidine ammonia-lyase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Intramural diverticulosis of esophagus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Ataxia-telangiectasia syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Hyperphenylalaninemia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital bronchopulmonary foregut malformation |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Limb reduction-ichthyosis syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Talipes planovalgus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital hypoplasia of pancreas |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Latent nystagmus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Xeroderma pigmentosum, group D |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Megaloblastic anemia due to error of cobalamin metabolism |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Situs inversus abdominalis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Tetrahydrobiopterin synthesis defect |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital keratoderma |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Juvenile taboparesis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Cystathionine gamma-lyase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital dyserythropoietic anemia, type II |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
| Triplet monster |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Hereditary benign intraepithelial dyskeratosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital mesenteroaxial volvulus of stomach |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Benign neonatal hyperaminoaciduria |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
| Double urethra |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Macrotia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Rothmund-Thomson syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital anomaly of fixation of intestine |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital aniridia (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Cleft lip sequence (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Macrodactylia of fingers |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Vascular hamartoma of skin |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Maroteaux-Lamy syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Pancreatic colipase deficiency |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Beaded hair |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital anomaly of digestive system |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Common atrium |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Hereditary orotic aciduria, type 1 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Adenosylcobalamin synthesis defect |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Combined immunodeficiency disease in Arab foals |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Proline dipeptidase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Ecchordosis physaliphora |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Unilobar lung |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital anomaly of esophagus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital occlusion of anus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Xanthoma tendinosum |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Residual ovary syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Persistent primary vitreous |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital absence of pulmonary valve |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Hereditary spherocytosis due to beta spectrin defect |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Asymmetrical conjoined twins (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Erythrokeratodermia variabilis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Fetal hydantoin syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital cubitus valgus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Atrial septal defect |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Anomaly of chromosome pair 21 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| 5p partial monosomy syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Hyperthermia-induced defect |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital anomaly of superior vena cava |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| I-cell disease |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital adhesions of tongue |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Horizontal overbite |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Crooked calf syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital anomaly of penis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital anomaly of heart valve |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| 15q partial trisomy syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| XTE syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Acrocephalosyndactyly type V (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Ectopic gastric tissue |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Anomaly of chromosome pair 22 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Hyperleucine-isoleucinemia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital dermal sinus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide-methemoglobin reductase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Mucolipidosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Occult spinal dysraphism sequence |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
| Streak ovary |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Incomplete development of membranous labyrinth |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Pseudocoarctation of aorta |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Ehlers-Danlos syndrome, recessive type 4 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Pygopagus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital discoid meniscus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Accessory salivary gland |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Mucopolysaccharidosis, MPS-II |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Bronchial atresia with segmental pulmonary emphysema |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital pseudoarthrosis of clavicle (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Single monster |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Longitudinal deficiency of upper limb |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Allemann's syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Meningomyelocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital absence of rib |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Situs inversus thoracis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Multiseptate gallbladder |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Dicheirus (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Omental cyst |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Congenital absence of upper arm AND forearm |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
| Congenital spinal hydromeningocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Tay-Sachs disease, variant AB |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital kyphosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Familial articular hypermobility syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
| Osteogenesis imperfecta, dominant perinatal lethal |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|