Infantile spasms

Symptom Information:

Symptom ID: HPO:0012469
Synonyms:
Infantile spasms [OMIM:Infantile spasms]
Infantile spasm [OMIM:Infantile spasm]
Infantile spasms [MedDRA:10021750]
Quality:
Cross references:
OMIM: "Infantile spasms" [OMIM:Infantile spasms]
OMIM: "Infantile spasm" [OMIM:Infantile spasm]
Is a (Direct Parents):
HPO         Epileptic spasms
MedDRA Seizures and seizure disorders NEC
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)