Developmental delay, profound

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Developmental delay, profound" [OMIM:Developmental delay, profound]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Congenital ichthyosis - intellectual deficit - spastic quadriplegia (Orphanet:352333)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A (OMIM:277470)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)
Porencephaly-microcephaly-bilateral congenital cataract syndrome (Orphanet:306547)