Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Flaccidity of muscle |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Floppy muscles |
Is a |
False |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Muscle tone atonic |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal hypotonia |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acquired hypotonia (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Puerto Rican infant hypotonia syndrome (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cystinuria, type 1 |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Benign congenital hypotonia (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypotonic-hyporesponsive episode (finding) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Allan-Herndon-Dudley syndrome |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Intellectual disability, epilepsy, extrapyramidal syndrome |
Is a |
True |
Poor muscle tone |
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 |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
GNAO1-related developmental delay, seizures, movement disorder spectrum |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Chloride voltage-gated channel 6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Appendicular hypotonia (finding) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Episodic hypotonia |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypotonia of axial muscles occurring in infancy |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypotonia of muscles of mouth region (finding) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypotonia of muscle of face (finding) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
2p21 microdeletion syndrome without cystinuria (disorder) |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Severe hypotonia of muscle |
Is a |
True |
Poor muscle tone |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|