Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Decreased gastric tonus (finding) |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
On examination - muscle tone hypotonic |
Associated finding |
False |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Traumatic hypotonia (disorder) |
Has definitional manifestation |
False |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
On examination - muscle tone hypotonic |
Is a |
False |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Decreased muscle tone - right side more than left side (finding) |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Decreased muscle tone - left side more than right side |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Benign congenital hypotonia (disorder) |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Traumatic hypotonia (disorder) |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome is a rare, genetic, non-dystrophic congenital myopathy disorder characterized by a neonatal-onset of severe generalized hypotonia associated with mild psychomotor delay, congenital strabismus with abducens nerve palsy, and atrial and/or ventricular septal defects. Cryptorchidism is commonly reported in male patients and muscle biopsy typically reveals increased variability in muscle fiber size. |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Allan-Herndon-Dudley syndrome |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
GNAO1-related developmental delay, seizures, movement disorder spectrum |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome (disorder) |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Episodic hypotonia |
Is a |
True |
Decreased muscle tone (finding) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|