Developmental delay, profound
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 6 / 7739 | |
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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) |