Developmental delay, severe

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Developmental delay, severe (2p21del) [OMIM:Developmental delay, severe (2p21del)]
Quality:
Cross references:
OMIM: "Developmental delay, severe" [OMIM:Developmental delay, severe]
OMIM: "Developmental delay, severe (2p21del)" [OMIM:Developmental delay, severe (2p21del)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 13 / 7739
Resource:

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)