Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
14q11.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay, hypotonia and facial dysmorphism. |
Is a |
False |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
14q12 microdeletion syndrome is a recently described syndrome characterized by severe intellectual deficit, with a normal neonatal period, followed by a phase of regression at the age of 3-6 months. |
Is a |
False |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
Distal monosomy 14q is a rare chromosomal anomaly associated with various phenotypic features depending on the size of the deletion. The clinical features may include global developmental delay, hypotonia, congenital heart defects, dysmorphic features (high forehead, small palpebral fissures, epicanthi, blepharophimosis, broad and flat nasal bridge, broad philtrum, thin upper lip, high arched palate, pointed chin, malformed ears). High-pitched, weak cry, seizures and various dental and ophthalmological anomalies were also reported. |
Is a |
False |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
14q22q23 microdeletion syndrome is a rare partial deletion of the long arm of chromosome 14 characterized by ocular anomalies (anophthalmia/microphthalmia, ptosis, hypertelorism, exophthalmos), pituitary anomalies (pituitary hypoplasia/aplasia with growth hormone deficiency and growth retardation) and hand/foot anomalies (polydactyly, short digits, pes cavus). Other clinical features may include muscular hypotonia, psychomotor development delay/intellectual disability, dysmorphic signs (facial asymmetry, microretrognathia, high-arched palate, ear anomalies), congenital genitourinary malformations, hearing impairment. Smaller 14q22 deletions may have variable expression. |
Is a |
False |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
14q24.1q24.3 microdeletion syndrome is a rare, genetic, syndromic intellectual disability characterized by mild intellectual disability, delayed speech development, congenital heart defects, brachydactyly and dysmorphic facial features. |
Is a |
False |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
14q32 deletion syndrome |
Is a |
False |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
Distal deletion of chromosome 14 (disorder) |
Is a |
True |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
Paternal 14q32.2 microdeletion (disorder) |
Is a |
False |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
Medial deletion of chromosome 14 |
Is a |
True |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
Proximal deletion of chromosome 14 |
Is a |
True |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|
Partial deletion of long arm of chromosome 14 (disorder) |
Is a |
True |
Deletion of part of chromosome 14 (disorder) |
Inferred relationship |
Some |
|