Female
Yes
Yes
Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
NM_025114.4:c.4714G>T | 2 | NA |
Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
---|---|---|---|---|---|---|
610188.4 | Saudi Arabia | Global developmental delay; Intellectual disability; Seizure; Abnormal posterior cranial fossa morphology | Female | Yes | Yes | Affected sibling |
610188.5 | Saudi Arabia | Generalized hypotonia; Global developmental delay; Visual impairment; Nystagmus | Female | Yes | ||
610188.6 | Saudi Arabia | Retinal dystrophy; Nephronophthisis; Molar tooth sign on MRI | Female | Yes | ||
610188.7 | Saudi Arabia | Global developmental delay; Molar tooth sign on MRI | Female | Yes | Yes | |
610188.9 | Saudi Arabia | Molar tooth sign on MRI | Unknown | |||
610188.10 | Saudi Arabia | Molar tooth sign on MRI; Nephronophthisis | Unknown | |||
610188.11 | Saudi Arabia | Ataxia; Molar tooth sign on MRI; Global developmental delay; Hypotonia | Unknown | Yes | Patient from 'JS_F11' family in the publication | |
610188.12 | Saudi Arabia | Ataxia; Molar tooth sign on MRI; Global developmental delay; Hypotonia | Unknown | Yes | Patient from 'MTI_587' family in the publication | |
610188.13 | Saudi Arabia | Ataxia; Molar tooth sign on MRI; Global developmental delay; Hypotonia | Unknown | Yes | Patient from 'MTI_012' family in the publication |