Polymicrogyria
Symptom Information:
Symptom ID: | HPO:0002126 | |||||||||||
Synonyms: |
|
|||||||||||
Quality: | ||||||||||||
Cross references: |
|
|||||||||||
Is a (Direct Parents): |
|
|||||||||||
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) |