LD20.2
category
Syndromes with microcephaly as a major feature
Definition
Developmental syndromes in which an abnormally small head size is a significant feature.
Also indexed as
Bowen-Conradi syndromeCongenital intrauterine infection-like syndromeIntellectual development disorder and microcephaly with pontine and cerebellar hypoplasiaMICPCH - [mental retardation and microcephaly with pontine and cerebellar hypoplasia]MOPD - [microcephalic osteodysplastic primordial dwarfism] types 1 and 3MPOD - [microcephalic osteodysplastic primordial dwarfism] type 2Microcephalic osteodysplastic primordial dwarfism type 2Microcephalic osteodysplastic primordial dwarfism type IIMicrocephalic osteodysplastic primordial dwarfism types 1 and 3Microcephalic osteodysplastic primordial short stature type 2Microcephalic osteodysplastic primordial short stature types 1 and 3Microcephaly - brain defect - spasticity - hypernatremiaMicrocephaly - cervical spine fusion anomaliesMicrocephaly, Amish typeMicrocephaly-microcornea syndrome, Seemanova typeMitochondrial thiamine pyrophosphate carrier deficiencyPseudo-TORCH syndromeSevere neonatal-onset encephalopathy with microcephalySyndromes with microcephaly as a major feature
Nearby in Syndromes with central nervous system anomalies as a major feature
LD20.0Syndromes with cerebellar anomalies as a major featureLD20.1Syndromes with lissencephaly as a major featureLD20.3Syndromes with holoprosencephaly as a major featureLD20.4Syndromes with brain calcifications as a major feature4B4YOther specified diseases of the immune system4B4ZDiseases of the immune system, unspecified