Disease #03326 (MCSZ;EIEE10 (microcephaly, seizures, and developmental delay (MCSZ, encephalopathy, epileptic, early infantile, type 10)), OMIM:613402)
| Official abbreviation |
MCSZ;EIEE10 |
| Name |
microcephaly, seizures, and developmental delay (MCSZ, encephalopathy, epileptic, early infantile, type 10) |
| OMIM ID |
613402 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
PNKP |
| Associated tissues |
- |
| Disease features |
onset infancy, no cerebellar ataxia (-HP:0001251), no cerebellar atrophy (-HP:0001272), no peripheral neuropathy (-HP:0009830), no muscle weakness (-HP:0001324), developmental delay (HP:0001263), seizures (HP:0001250), no hyporeflexia (-HP:0001265), cognitive impairment (HP:0100543), no oculomotor apraxia (-HP:0000657), no dystonia (-HP:0001332) |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2024-09-10 21:09:25 +02:00 (CEST) |
Individuals
|