microcephaly - CISMeF

Preferred Label : microcephaly;

MeSH definition : A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.);

MeSH synonym : microcephalies;

MeSH hyponym : Severe Congenital Microcephaly; Congenital Microcephalies, Severe; Congenital Microcephaly, Severe; Microcephalies, Severe Congenital; Microcephaly, Severe Congenital; Severe Congenital Microcephalies;

Related MeSH term : microlissencephaly; Microlissencephalies;

Wikipedia link : https://en.wikipedia.org/wiki/Microcephaly;

Details

Origin ID

D008831;

UMLS CUI

C0025958;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Microlissencephaly [ICD-11 More detail]
- Microlissencephaly [HPO term]
DO Cross reference
- microcephaly [DO Concept]
False automatic mappings
- Lissencephaly syndrome, Norman-Roberts type [ORDO Disease]
- Microlissencephaly [ORDO Disease]
- Microlissencephaly (disorder) [SNOMED CT concept]
Manual NTBT mappings (CISMeF)
- abnormal head size [Disease (Nov.)]
Record concept(s)
- Severe Congenital Microcephaly [MeSH concept]
- microcephaly [MeSH concept]
- microlissencephaly [MeSH concept]
Related MeSH Supplementary Concept(s)
- Ataxia-Microcephaly-Cataract syndrome [MeSH Supplementary Concept]
- Baetz-Greenwalt syndrome [MeSH Supplementary Concept]
- CAMFAK syndrome [MeSH Supplementary Concept]
- GOMBO syndrome [MeSH Supplementary Concept]
- Hypospadias-Mental retardation syndrome [MeSH Supplementary Concept]
- MEHMO syndrome [MeSH Supplementary Concept]
- MacDermot winter syndrome [MeSH Supplementary Concept]
- Microcephaly-Micromelia syndrome [MeSH Supplementary Concept]
- Mowat-Wilson syndrome [MeSH Supplementary Concept]
- absent eyebrows and eyelashes with mental retardation [MeSH Supplementary Concept]
- achalasia microcephaly [MeSH Supplementary Concept]
- agammaglobulinemia, microcephaly, and severe dermatitis [MeSH Supplementary Concept]
- alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus [MeSH Supplementary Concept]
- amish lethal microcephaly [MeSH Supplementary Concept]
- anonychia, total, with microcephaly [MeSH Supplementary Concept]
- aphalangia syndactyly microcephaly [MeSH Supplementary Concept]
- autosomal recessive primary microcephaly [MeSH Supplementary Concept]
- baraitser brett piesowicz syndrome [MeSH Supplementary Concept]
- battaglia neri syndrome [MeSH Supplementary Concept]
- bixler christian gorlin syndrome [MeSH Supplementary Concept]
- boudhina yedes khiari syndrome [MeSH Supplementary Concept]
- brachydactyly, type A2, with microcephaly [MeSH Supplementary Concept]
- branchial arch syndrome X-linked [MeSH Supplementary Concept]
- bullous dystrophy, hereditary macular type [MeSH Supplementary Concept]
- cardiac malformation, cleft Lip-Palate, microcephaly and digital anomalies [MeSH Supplementary Concept]
- cataract, microcephaly, arthrogryposis, kyphosis syndrome [MeSH Supplementary Concept]
- chromosomal instability with Tissue-Specific radiosensitivity [MeSH Supplementary Concept]
- chromosome 15q26-Qter deletion syndrome [MeSH Supplementary Concept]
- cohen syndrome [MeSH Supplementary Concept]
- craniosynostosis microcephaly with chromosomal breakage and other abnormalities [MeSH Supplementary Concept]
- dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation [MeSH Supplementary Concept]
- dubowitz syndrome [MeSH Supplementary Concept]
- ellis yale winter syndrome [MeSH Supplementary Concept]
- encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration [MeSH Supplementary Concept]
- extrasystoles, multiform ventricular, with short stature, hyperpigmentation and microcephaly [MeSH Supplementary Concept]
- filippi syndrome [MeSH Supplementary Concept]
- galloway mowat syndrome [MeSH Supplementary Concept]
- growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate [MeSH Supplementary Concept]
- growth deficiency and mental retardation with facial dysmorphism [MeSH Supplementary Concept]
- hadziselimovic syndrome [MeSH Supplementary Concept]
- halal syndrome [MeSH Supplementary Concept]
- hersh podruch weisskopk syndrome [MeSH Supplementary Concept]
- hoyeraal hreidarsson syndrome [MeSH Supplementary Concept]
- hypogonadism with Low-Grade mental deficiency and microcephaly [MeSH Supplementary Concept]
- jejunal atresia with microcephaly and ocular anomalies [MeSH Supplementary Concept]
- jorgenson lenz syndrome [MeSH Supplementary Concept]
- kaufman oculocerebrofacial syndrome [MeSH Supplementary Concept]
- lambotte syndrome [MeSH Supplementary Concept]
- lissencephaly 3 [MeSH Supplementary Concept]
- lowry wood syndrome [MeSH Supplementary Concept]
- lymphedema, microcephaly and chorioretinopathy syndrome [MeSH Supplementary Concept]
- marfanoid habitus with microcephaly and glomerulonephritis [MeSH Supplementary Concept]
- mental retardation and microcephaly with pontine and cerebellar hypoplasia [MeSH Supplementary Concept]
- mental retardation, X-Linked, syndromic 9 [MeSH Supplementary Concept]
- mental retardation, X-Linked, syndromic, christianson type [MeSH Supplementary Concept]
- mental retardation, microcephaly, epilepsy, and coarse face [MeSH Supplementary Concept]
- microcephalic osteodysplastic primordial dwarfism, type 1 [MeSH Supplementary Concept]
- microcephalic osteodysplastic primordial dwarfism, type 3 [MeSH Supplementary Concept]
- microcephalic osteodysplastic primordial dwarfism, type II [MeSH Supplementary Concept]
- microcephalic primordial dwarfism toriello type [MeSH Supplementary Concept]
- microcephaly albinism digital anomalies syndrome [MeSH Supplementary Concept]
- microcephaly autosomal dominant [MeSH Supplementary Concept]
- microcephaly cervical spine fusion anomalies [MeSH Supplementary Concept]
- microcephaly deafness syndrome [MeSH Supplementary Concept]
- microcephaly microphthalmos blindness [MeSH Supplementary Concept]
- microcephaly nonsyndromal [MeSH Supplementary Concept]
- microcephaly pontocerebellar hypoplasia dyskinesia [MeSH Supplementary Concept]
- microcephaly seizures genital hypoplasia [MeSH Supplementary Concept]
- microcephaly seizures mental retardation heart disorders [MeSH Supplementary Concept]
- microcephaly sparse hair mental retardation seizures [MeSH Supplementary Concept]
- microcephaly with chemotactic defect and transient hypogammaglobulinemia [MeSH Supplementary Concept]
- microcephaly with chorioretinopathy, autosomal dominant [MeSH Supplementary Concept]
- microcephaly with chorioretinopathy, autosomal recessive [MeSH Supplementary Concept]
- microcephaly with mental retardation and digital anomalies [MeSH Supplementary Concept]
- microcephaly with simplified gyral pattern [MeSH Supplementary Concept]
- microcephaly with spastic quadriplegia [MeSH Supplementary Concept]
- microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs [MeSH Supplementary Concept]
- microcephaly, corpus callosum dysgenesis and cleft lip-palate [MeSH Supplementary Concept]
- microcephaly, growth retardation, cataract, hearing loss, and unusual appearance [MeSH Supplementary Concept]
- microcephaly, macrotia, and mental retardation [MeSH Supplementary Concept]
- microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MeSH Supplementary Concept]
- microcephaly, primary autosomal recessive, 1 [MeSH Supplementary Concept]
- microcephaly, primary autosomal recessive, 2 [MeSH Supplementary Concept]
- microcephaly, primary autosomal recessive, 3 [MeSH Supplementary Concept]
- microcephaly, primary autosomal recessive, 4 [MeSH Supplementary Concept]
- microcephaly, primary autosomal recessive, 5 [MeSH Supplementary Concept]
- microcephaly, primary autosomal recessive, 5, with simplified gyral pattern [MeSH Supplementary Concept]
- microcephaly, primary autosomal recessive, 6 [MeSH Supplementary Concept]
- microcephaly, primary autosomal recessive, 7 [MeSH Supplementary Concept]
- microcephaly, retinitis pigmentosa, and sutural cataract [MeSH Supplementary Concept]
- microcephaly, severe, with skeletal anomalies including posterior Rib-Gap defects [MeSH Supplementary Concept]
- microhydranencephaly [MeSH Supplementary Concept]
- microphthalmia and mental deficiency [MeSH Supplementary Concept]
- milner khallouf gibson syndrome [MeSH Supplementary Concept]
- muscular dystrophy, congenital, associated with calf hypertrophy, microcephaly, and severe mental retardation [MeSH Supplementary Concept]
- neu laxova syndrome [MeSH Supplementary Concept]
- nijmegen breakage Syndrome-Like disorder [MeSH Supplementary Concept]
- oculodigitoesophagoduodenal syndrome [MeSH Supplementary Concept]
- oculopalatocerebral syndrome [MeSH Supplementary Concept]
- osteogenesis imperfecta congenita, microcephaly, and cataracts [MeSH Supplementary Concept]
- paine syndrome [MeSH Supplementary Concept]
- partington anderson syndrome [MeSH Supplementary Concept]
- phosphoglycerate dehydrogenase deficiency [MeSH Supplementary Concept]
- phosphoserine aminotransferase deficiency [MeSH Supplementary Concept]
- raine syndrome [MeSH Supplementary Concept]
- sammartino de crecchio syndrome [MeSH Supplementary Concept]
- say barber miller syndrome [MeSH Supplementary Concept]
- say syndrome [MeSH Supplementary Concept]
- schimke X-linked mental retardation syndrome [MeSH Supplementary Concept]
- seckel syndrome 1 [MeSH Supplementary Concept]
- seckel syndrome 2 [MeSH Supplementary Concept]
- seckel syndrome 3 [MeSH Supplementary Concept]
- secretory diarrhea, myopathy, and deafness [MeSH Supplementary Concept]
- seemanova lesny syndrome [MeSH Supplementary Concept]
- severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation [MeSH Supplementary Concept]
- silengo lerone pelizza syndrome [MeSH Supplementary Concept]
- spastic paraplegia, optic atrophy, microcephaly, and xy sex reversal [MeSH Supplementary Concept]
- spinal muscular atrophy with microcephaly and mental subnormality [MeSH Supplementary Concept]
- spondyloepimetaphyseal dysplasia, genevieve type [MeSH Supplementary Concept]
- teebi kaurah syndrome [MeSH Supplementary Concept]
- trichodental syndrome [MeSH Supplementary Concept]
- tsukahara syndrome [MeSH Supplementary Concept]
- warburg sjo fledelius syndrome [MeSH Supplementary Concept]
- warburton anyane yeboa syndrome [MeSH Supplementary Concept]
- winship viljoen leary syndrome [MeSH Supplementary Concept]
- zerres rietschel majewski syndrome [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- lissencephaly [MeSH Descriptor]
See also inter- (CISMeF)
- Microcephaly (finding) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Isolated congenital microcephaly [ORDO Disease]
- MICROCEPHALY [WHO-ART High Level Term]
- Microcephalic [MedDRA LLT]
- Microcephalus [ICD-9 code]
- Microcephalus [MedDRA LLT]
- Microcephalus (disorder) [SNOMED CT concept]
- Microcephaly [MedDRA Preferred Term]
- Microcephaly [ICD-10 category]
- Microcephaly [ICD-10 category (who)]
- Microcephaly [HRDO Sign]
- Microcephaly [NCIt concept]
- Microencephaly [MedDRA Preferred Term]
- microcephalus [SNOMED Notion]
- microcephaly [DO Concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients