Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Global developmental delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Development delay NOS |
Is a |
False |
Developmental delay |
Inferred relationship |
Some |
|
Cognitive developmental delay (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Developmental delay in feeding (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Developmental delay in fine motor function (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Developmental delay in social skills |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Family history of neurological developmental delay |
Associated finding |
True |
Developmental delay |
Inferred relationship |
Some |
1 |
Koolen De Vries syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Cardiocranial syndrome Pfeiffer type (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Bohring Opitz syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Frank-Ter Haar syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Trigonocephaly, short stature, developmental delay syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Cyclin-dependent kinase-like 5 deficiency (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Congenital cataract, hearing loss, severe developmental delay syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Pancytopenia with developmental delay syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Lethal polymalformative syndrome Boissel type |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Xp22.13p22.2 duplication syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder) |
Is a |
False |
Developmental delay |
Inferred relationship |
Some |
|
Delay in sexual development AND/OR puberty |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Phonological delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Speech delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Expressive language delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Receptive language delay (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Delayed pre-verbal development |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Clumsiness - motor delay |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Gross motor development delay (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
PPM-X syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Developmental delay in receptive-expressive language (disorder) |
Is a |
False |
Developmental delay |
Inferred relationship |
Some |
|
Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Cutis laxa-corneal clouding-oligophrenia syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Proximal 16p11.2 microdeletion syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Distal 16p11.2 microdeletion syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Beta-D-mannosidosis |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome (disorder) |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|
Spastic paraplegia, severe developmental delay, epilepsy syndrome |
Is a |
True |
Developmental delay |
Inferred relationship |
Some |
|