Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Feeding problem in child |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|
Feeding problem symptom |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|
Elderly feeding problem |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|
Feeding problem due to illness (finding) |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|
Underfeeding in newborn |
Is a |
False |
Feeding problem |
Inferred relationship |
Some |
|
Overfeeding in newborn |
Is a |
False |
Feeding problem |
Inferred relationship |
Some |
|
Bottle feeding problem in the newborn |
Is a |
False |
Feeding problem |
Inferred relationship |
Some |
|
Breastfeeding problem in the newborn (finding) |
Is a |
False |
Feeding problem |
Inferred relationship |
Some |
|
Poor feeding of newborn |
Is a |
False |
Feeding problem |
Inferred relationship |
Some |
|
Feeding poor |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|
Ineffective infant feeding pattern |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|
Difficulty in feeding at breast |
Is a |
False |
Feeding problem |
Inferred relationship |
Some |
|
Feeding problem in adulthood (finding) |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|
A rare pervasive developmental disorder characterized by microcephaly, profound developmental delay, intellectual disability, bilateral cataracts, severe epilepsy including infantile spasms, hypotonia, irritability, feeding difficulties leading to failure to thrive, and stereotypic hand movements. The disease manifests in infancy. Brain imaging reveals delay in myelination and cerebral atrophy. |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|
Feeding problems in newborn |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|
A rare syndromic intellectual disability without congenital anomalies/specific dysmorphic phenotype characterised by delayed psychomotor development, severe intellectual disability, delayed or absent speech development, hypotonia, ataxic gait and feeding difficulties. Clinical symptoms are evident from early infancy. Majority of the patients also present with behavioural abnormalities (including autistic features, aggressive behaviour, low frustration tolerance, and stereotypies such as hand-flapping). Additional clinical features may include inability to walk, seizures, hearing loss, sleep abnormalities, joint hyperlaxity. Nonspecific dysmorphic facial features (small head, strabismus, epicanthal folds, synophrys, high palate, low-set ears, orofacial hypotonia, full eyelids, and eversion of the lower lip) may also be present. |
Is a |
True |
Feeding problem |
Inferred relationship |
Some |
|