| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Global developmental delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Development delay NOS |
Is a |
False |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Cognitive developmental delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Developmental delay in feeding |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Developmental delay in fine motor function |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Developmental delay in social skills |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Family history of neurological developmental delay |
Associated finding |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
1 |
| Koolen De Vries syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Cardiocranial syndrome Pfeiffer type |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Bohring Opitz syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Frank-Ter Haar syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Developmental delay, epilepsy, neonatal diabetes syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Trigonocephaly, short stature, developmental delay syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Cyclin-dependent kinase-like 5 deficiency |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Spondyloepimetaphyseal dysplasia Genevieve type |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Congenital cataract, hearing loss, severe developmental delay syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Pancytopenia with developmental delay syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Lethal polymalformative syndrome Boissel type |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Xp22.13p22.2 duplication syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion |
Is a |
False |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Delay in sexual development AND/OR puberty |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Phonological delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Speech delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Expressive language delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Receptive language delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Delayed pre-verbal development |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Clumsiness - motor delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Gross motor development delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| X-linked intellectual disability-psychosis-macroorchidism syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Developmental delay in receptive-expressive language |
Is a |
False |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Severe achondroplasia, developmental delay, acanthosis nigricans syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Cutis laxa-corneal clouding-oligophrenia syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Proximal 16p11.2 microdeletion syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Distal 16p11.2 microdeletion syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Beta-D-mannosidosis |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Spastic paraplegia, severe developmental delay, epilepsy syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Congenital ichthyosis, microcephalus, tetraplegia syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Special AT-rich sequence-binding protein 2-associated syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Joint contractures, developmental delay, Pierre Robin syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Ring finger protein 13-related severe early-onset epileptic encephalopathy |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| 1p35.2 microdeletion syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| 9q33.3q34.11 microdeletion syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| 16p13.2 microdeletion syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Xq25 microduplication syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| 17q24.2 microdeletion syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| 11q22.2q22.3 microdeletion syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| 8q24.3 microdeletion syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Phosphodiesterase 4D haploinsufficiency syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| FG syndrome type 1 |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Oculocerebrodental syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Menke Hennekam syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Glutamate ionotropic receptor NMDA type subunit 2B-related developmental delay, intellectual disability, autism spectrum disorder |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Development delay NOS |
Is a |
False |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Neurodevelopmental delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|
| Motor developmental delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Existential restriction modifier |
|