Polymicrogyria

Symptom Information:

Symptom ID: HPO:0002126
Synonyms:
Polymicrogyria [Orphanet:42600]
Microgyria [Orphanet:42600]
Polymicrogyria [OMIM:Polymicrogyria]
Agyria/micro/pachy/macrogyria/lissencephaly/gyration/neuronal migration defect [Orphanet:42600]
Microgyria [OMIM:Microgyria]
Polymicrogyria (1 patient) [OMIM:Polymicrogyria (1 patient)]
Polymicrogyria (64%) [OMIM:Polymicrogyria (64%)]
Polymicrogyria (MEB) [OMIM:Polymicrogyria (MEB)]
Polymicrogyria (rare) [OMIM:Polymicrogyria (rare)]
Polymicrogyria (reported in 1 patient) [OMIM:Polymicrogyria (reported in 1 patient)]
Polymicrogyria [MedDRA:10073489]
Quality:
Cross references:
Orphanet:42600 "Agyria/micro/pachy/macrogyria/lissencephaly/gyration/neuronal migration defect" [Orphanet:42600]
OMIM: "Polymicrogyria" [OMIM:Polymicrogyria]
OMIM: "Microgyria" [OMIM:Microgyria]
OMIM: "Polymicrogyria (1 patient)" [OMIM:Polymicrogyria (1 patient)]
OMIM: "Polymicrogyria (64%)" [OMIM:Polymicrogyria (64%)]
OMIM: "Polymicrogyria (MEB)" [OMIM:Polymicrogyria (MEB)]
OMIM: "Polymicrogyria (rare)" [OMIM:Polymicrogyria (rare)]
OMIM: "Polymicrogyria (reported in 1 patient)" [OMIM:Polymicrogyria (reported in 1 patient)]
UMLS:C0266464 "Polymicrogyria" [HPO:0002126]
UMLS:C2362742 "Microgyria" [Orphanet:42600]
UMLS:C0266464 "Polymicrogyria" [Orphanet:42600]
Is a (Direct Parents):
HPO         Abnormal cortical gyration
Orphanet Pachygyria
MedDRA Congenital and peripartum cerebral disorders
Orphanet Structural anomalies of the nervous system
Is a (Whole tree): HPO:
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Congenital and peripartum neurological conditions(MedDRA:10010335)
       Congenital and peripartum cerebral disorders(MedDRA:10010334)
          Polymicrogyria(HPO:0002126)
Database Frequency: 64 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
ADAMS-OLIVER SYNDROME 1 (OMIM:100300)
ADAMS-OLIVER SYNDROME 2 (OMIM:614219)
Adams-Oliver syndrome (Orphanet:974)
Aicardi syndrome (Orphanet:50)
Autosomal recessive cutis laxa type 2, classic type (Orphanet:357074)
Autosomal recessive cutis laxa type 2A (Orphanet:357058)
Baller-Gerold syndrome (Orphanet:1225)
Bifunctional enzyme deficiency (Orphanet:300)
Bilateral generalized polymicrogyria (Orphanet:208447)
Bilateral perisylvian polymicrogyria (Orphanet:98889)
Bilateral polymicrogyria (Orphanet:268940)
CEDNIK syndrome (Orphanet:66631)
CEREBROOCULOFACIOSKELETAL SYNDROME 4 (OMIM:610758)
CK syndrome (Orphanet:251383)
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2 (OMIM:615282)
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6 (OMIM:615771)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Chudley-McCullough syndrome (Orphanet:314597)
Combined oxidative phosphorylation defect type 4 (Orphanet:254925)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Congenital muscular dystrophy type 1A (Orphanet:258)
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation (Orphanet:300570)
Diaphanospondylodysostosis (Orphanet:66637)
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY (OMIM:614520)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Fumaric aciduria (Orphanet:24)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Hypotonia-cerebral atrophy-hyperglycinemia syndrome (Orphanet:363424)
Joubert syndrome 2 (OMIM:608091)
Kapur-Toriello syndrome (Orphanet:2328)
Knobloch syndrome (Orphanet:1571)
LISSENCEPHALY 6 WITH MICROCEPHALY (OMIM:616212)
Lissencephaly due to TUBA1A mutation (Orphanet:171680)
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2 (OMIM:615937)
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 (OMIM:615938)
MELAS (Orphanet:550)
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS (OMIM:604317)
MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C (OMIM:615501)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 11 (OMIM:615181)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 (OMIM:613150)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 (OMIM:253280)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 (OMIM:253800)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 (OMIM:614643)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Microgastria - limb reduction defect (Orphanet:2538)
Muscle-eye-brain disease (Orphanet:588)
Nager syndrome (Orphanet:245)
PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER) (OMIM:614883)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) (OMIM:614866)
POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL (OMIM:612691)
Polymicrogyria with optic nerve hypoplasia (Orphanet:250972)
SRD5A3-CDG (Orphanet:324737)
Severe neonatal-onset encephalopathy with microcephaly (Orphanet:209370)
WARBURG MICRO SYNDROME 2 (OMIM:614225)
WARBURG MICRO SYNDROME 3 (OMIM:614222)
Wolcott-Rallison syndrome (Orphanet:1667)
Zellweger syndrome (Orphanet:912)