Male
No
No
Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
NM_000314.6:c.70G>C | 1 |
Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
---|---|---|---|---|---|---|
158350.1 | United Arab Emirates | Global developmental delay; Macrocephaly | Male | No | Yes | de novo mutation |
158350.3 | United Arab Emirates | Macrocephaly; Delayed speech and language development; Arachnoid cyst; Hamartoma; Lipoma; Gait disturbance | Female | No | Yes | de novo mutation |
158350.4 | United Arab Emirates | Microcephaly; Intellectual disability; Seizure; Cerebral atrophy; Scoliosis; Hip dislocation; Hyperpigmentation of the skin | Male | Yes | No |