Abnormality of neuronal migration

Symptom Information:

Symptom ID: HPO:0002269
Synonyms:
Abnormal neuronal migration [HPO:0002269]
Heterotopias/abnormal migration [HPO:0002269]
Migrational brain disorder [HPO:0002269]
Neuronal migration disorder [HPO:0002269]
Neuronal migration disorder [Orphanet:42600]
Neuronal Migration Disorders [Orphanet:42600]
Abnormal neuronal migration [OMIM:Abnormal neuronal migration]
Heterotopias/abnormal migration [OMIM:Heterotopias/abnormal migration]
Migrational brain disorder [OMIM:Migrational brain disorder]
Neuronal migration disorder [OMIM:Neuronal migration disorder]
Agyria/micro/pachy/macrogyria/lissencephaly/gyration/neuronal migration defect [Orphanet:42600]
Quality:
Cross references:
Orphanet:42600 "Agyria/micro/pachy/macrogyria/lissencephaly/gyration/neuronal migration defect" [Orphanet:42600]
OMIM: "Abnormal neuronal migration" [OMIM:Abnormal neuronal migration]
OMIM: "Heterotopias/abnormal migration" [OMIM:Heterotopias/abnormal migration]
OMIM: "Migrational brain disorder" [OMIM:Migrational brain disorder]
OMIM: "Neuronal migration disorder" [OMIM:Neuronal migration disorder]
UMLS:C1837249 "Neuronal Migration Disorders" [Orphanet:42600]
Is a (Direct Parents):
Orphanet Structural anomalies of the nervous system
Orphanet Pachygyria
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

3-hydroxyisobutyric aciduria (Orphanet:939)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT (OMIM:300049)
MELAS (Orphanet:550)
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS (OMIM:604317)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 (OMIM:608840)
Nodular neuronal heterotopia (Orphanet:2149)
PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) (OMIM:614887)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
Wolcott-Rallison syndrome (Orphanet:1667)