Phenotype #0000281002
Individual ID |
00387439 |
Associated disease |
MRD26 |
Phenotype details |
premature birth, low birth weight, feeding difficulties, intellectual disability/developmental delay, autism, generalized hypotonia, intraventricular hemorrhage, cerebral palsy/spasticity, hypertelorism, tight heel cords |
Diagnosis/Initial |
- |
Inheritance |
Isolated (sporadic) |
Diagnosis/Definite |
- |
Age/Examination |
07y02m (7 years, 2 months) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Birth_Details |
- |
Protein |
- |
Owner name |
Alexander Groffen |
Database submission license |
Creative Commons Attribution-ShareAlike 4.0 International |
Created by |
Alexander Groffen |
Date created |
2021-10-29 12:53:29 +02:00 (CEST) |
Date last edited |
N/A |
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