Developmental delay, mild

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Developmental delay, mild (in some patients) [OMIM:Developmental delay, mild (in some patients)]
Developmental delay, mild (in some) [OMIM:Developmental delay, mild (in some)]
Mild developmental delay [OMIM:Mild developmental delay]
Quality:
Cross references:
OMIM: "Developmental delay, mild" [OMIM:Developmental delay, mild]
OMIM: "Developmental delay, mild (in some patients)" [OMIM:Developmental delay, mild (in some patients)]
OMIM: "Developmental delay, mild (in some)" [OMIM:Developmental delay, mild (in some)]
OMIM: "Mild developmental delay" [OMIM:Mild developmental delay]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Char syndrome (Orphanet:46627)
Dent disease type 2 (Orphanet:93623)
Developmental malformations - deafness - dystonia (Orphanet:79107)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Leukoencephalopathy - ataxia - hypodontia - hypomyelination (Orphanet:137639)
Odontoleukodystrophy (Orphanet:77295)
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME (OMIM:601321)