Infantile spasms
Symptom Information:
Symptom ID: | HPO:0012469 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Seizures(HPO:0001250) Epileptic spasms(HPO:0011097) Infantile spasms(HPO:0012469) MedDRA: Nervous system disorders(MedDRA:10029205) Seizures(HPO:0001250) Seizures and seizure disorders NEC(MedDRA:10039912) Infantile spasms(HPO:0012469) |
||||
Database Frequency: | 18 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Aicardi syndrome | (Orphanet:50) |
Atypical Rett syndrome | (Orphanet:3095) |
CEREBROOCULOFACIOSKELETAL SYNDROME 1 | (OMIM:214150) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx | (OMIM:212067) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
Leigh syndrome | (Orphanet:506) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Miller-Dieker syndrome | (Orphanet:531) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
TUBEROUS SCLEROSIS 1 | (OMIM:191100) |
TUBEROUS SCLEROSIS 2 | (OMIM:613254) |
Tuberous sclerosis | (Orphanet:805) |
West syndrome | (Orphanet:3451) |