Developmental delay, severe
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Database Frequency: | 13 / 7739 | ||
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All diseases associated with this symptom:
2p21 microdeletion syndrome | (Orphanet:163693) |
Atypical hypotonia - cystinuria syndrome | (Orphanet:238523) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET | (OMIM:114100) |
D-2-@HYDROXYGLUTARIC ACIDURIA 1 | (OMIM:600721) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Lethal polymalformative syndrome, Boissel type | (Orphanet:210144) |
Lissencephaly due to LIS1 mutation | (Orphanet:95232) |
Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
Phosphoenolpyruvate carboxykinase 1 deficiency | (Orphanet:79316) |
Polymicrogyria with optic nerve hypoplasia | (Orphanet:250972) |
Pontocerebellar hypoplasia type 3 | (Orphanet:97249) |
Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome | (Orphanet:306558) |
Severe neonatal-onset encephalopathy with microcephaly | (Orphanet:209370) |