| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Nievergelt's syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Nievergelt's syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Autosomal recessive Robinow syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 7 | 
| Autosomal dominant Robinow syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 7 | 
| Autosomal recessive Robinow syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Brachydactyly type A6 (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Congenital trigger finger | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Pediatric locking of interphalangeal joint of right thumb (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Pediatric trigger thumb of left hand | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Pediatric locking of interphalangeal joint of bilateral thumbs (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Pediatric locking of interphalangeal joint of bilateral thumbs (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Pediatric trigger thumb | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Locked pediatric trigger thumb | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Multiple epiphyseal dysplasia Lowry type (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Cleidorhizomelic syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 3 | 
| Multiple epiphyseal dysplasia Lowry type (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 6 | 
| Perimembranous outlet ventricular septal defect with posteriorly malaligned outlet septum (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Perimembranous inlet ventricular septal defect (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Perimembranous inlet ventricular septal defect with atrioventricular septal malalignment (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 3 | 
| Perimembranous ventricular septal defect | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Central basal perimembranous ventricular septal defect (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Perimembranous outlet ventricular septal defect with anteriorly malaligned outlet septum (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 3 | 
| True cleft of left atrioventricular valve leaflet | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Zechi Ceide syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 8 | 
| Perimembranous outlet ventricular septal defect with posteriorly malaligned outlet septum (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 3 | 
| Autosomal dominant osteopetrosis type 1 | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Aplasia of external auditory canal (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Persistent left superior vena cava connecting through coronary sinus to left sided atrium | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Fetal trimethadione syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital non-syndromic anorectal malformation (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Arthrogryposis multiplex congenita | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Marden Walker syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Marden Walker syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Microphthalmia, microtia, fetal akinesia syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 6 | 
| Congenital muscular dystrophy with arthrogryposis multiplex congenita | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 6 | 
| Congenital amyoplasia (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital radioulnar synostosis | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital radioulnar synostosis | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Congenital malposition of left external ear (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital malposition of right external ear (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Usher syndrome type 1F (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Congenital split of bilateral ear lobes (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital split of bilateral ear lobes (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Craniosynostosis, microretrognathia, severe intellectual disability syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Craniosynostosis, microretrognathia, severe intellectual disability syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Spondylometaphyseal dysplasia, corneal dystrophy syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Spondylometaphyseal dysplasia, corneal dystrophy syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 3 | 
| Spondylometaphyseal dysplasia, corneal dystrophy syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Primary hypomagnesemia, refractory seizures, intellectual disability syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Lennox-Gastaut syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Symptomatic Lennox-Gastaut syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Infantile epileptic dyskinetic encephalopathy (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Myoclonic epilepsy in non-progressive encephalopathy | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Cryptogenic Lennox-Gastaut syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Developmental and epileptic encephalopathy | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 6 | 
| Epileptic encephalopathy (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Congenital velopharyngeal dysfunction | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital incomplete closure of velopharyngeal apparatus due to anatomical abnormality (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Embryonic cyst of right ovary (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Embryonic cyst of left ovary | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital anomaly of left fallopian tube | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital anomaly of right fallopian tube (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Embryonic cyst of left fallopian tube | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Embryonic cyst of right fallopian tube (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Neonatal epileptic encephalopathy due to glutaminase deficiency | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 3 | 
| Myoclonic encephalopathy | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Early infantile epileptic encephalopathy with suppression bursts | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Epilepsy with continuous spike wave during slow-wave sleep | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Syntaxin binding protein 1 encephalopathy with epilepsy (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Epilepsy with myoclonic-atonic seizures (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital insensitivity to pain, anosmia, neuropathic arthropathy | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 5 | 
| Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 6 | 
| Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 7 | 
| Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 8 | 
| Congenital cataract microcornea with corneal opacity | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Congenital cataract microcornea with corneal opacity | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Congenital cataract microcornea with corneal opacity | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 3 | 
| Short rib polydactyly syndrome type 5 | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Short rib polydactyly syndrome type 5 | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Short rib polydactyly syndrome type 5 | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 3 | 
| Short rib polydactyly syndrome type 5 | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Combined oxidative phosphorylation defect type 39 | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Laminin alpha-2 related limb girdle muscular dystrophy R23 (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Calpain-3-related limb girdle muscular dystrophy D4 | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 | 
| Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 2 | 
| Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 3 | 
| Multiple mitochondrial dysfunctions syndrome type 6 (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 4 | 
| Rupture of congenital aneurysm of cerebral artery (disorder) | Pathological process (attribute) | True | Pathological developmental process | Inferred relationship | Some | 1 |