Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Flaccidity of muscle (finding) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Floppy muscles |
Is a |
False |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Muscle tone atonic |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Neonatal hypotonia |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Acquired hypotonia |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (disorder) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Puerto Rican infant hypotonia syndrome (disorder) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Cystinuria, type 1 |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Benign congenital hypotonia |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Hypotonic-hyporesponsive episode (finding) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Allan-Herndon-Dudley syndrome |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Intellectual disability, epilepsy, extrapyramidal syndrome |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum (disorder) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Chloride voltage-gated channel 6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome (disorder) |
Is a |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
|
Acute flaccid paraparesis (disorder) |
Associated with |
True |
Poor muscle tone (finding) |
Inferred relationship |
Some |
2 |