Phenotype #0000025744
| Individual ID |
00029780 |
| Associated disease |
AOS |
| Phenotype details |
IUGR; scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); microcephaly; microphthalmia; retinal detachment; anterior chamber abnormality; severe ID; seizures / epilepsy; cerebral palsy / spasticity; CMTC; abdominal skin defect; |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
20y00m (20 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Maja Sukalo |
| Database submission license |
No license selected |
| Created by |
Maja Sukalo |
| Date created |
2015-01-28 18:24:22 +01:00 (CET) |
| Date last edited |
2015-02-07 16:02:48 +01:00 (CET) |
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