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