Delayed psychomotor development, severe

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Delayed psychomotor development, severe (> 90%) [OMIM:Delayed psychomotor development, severe (> 90%)]
Delayed psychomotor development, severe (in 2 of 6 patients) [OMIM:Delayed psychomotor development, severe (in 2 of 6 patients)]
Quality:
Cross references:
OMIM: "Delayed psychomotor development, severe" [OMIM:Delayed psychomotor development, severe]
OMIM: "Delayed psychomotor development, severe (> 90%)" [OMIM:Delayed psychomotor development, severe (> 90%)]
OMIM: "Delayed psychomotor development, severe (in 2 of 6 patients)" [OMIM:Delayed psychomotor development, severe (in 2 of 6 patients)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Allan-Herndon-Dudley syndrome (Orphanet:59)
Beta-ureidopropionase deficiency (Orphanet:65287)
Bifunctional enzyme deficiency (Orphanet:300)
Cystic leukoencephalopathy without megalencephaly (Orphanet:85136)
Desmosterolosis (Orphanet:35107)
Epileptic encephalopathy with global cerebral demyelination (Orphanet:353217)
Fatal infantile lactic acidosis with methylmalonic aciduria (Orphanet:17)
Infantile cerebellar-retinal degeneration (Orphanet:313850)
Intellectual deficit, X-linked, Cantagrel type (Orphanet:85277)
Joubert syndrome 20 (OMIM:614970)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 11 (OMIM:615181)
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM (OMIM:614501)
Pontocerebellar hypoplasia type 7 (Orphanet:284339)
Pontocerebellar hypoplasia type 8 (Orphanet:324569)