Vision impairment, progressive

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Vision impairment, progressive (onset in late childhood, teens) [OMIM:Vision impairment, progressive (onset in late childhood, teens)]
Quality:
Cross references:
OMIM: "Vision impairment, progressive" [OMIM:Vision impairment, progressive]
OMIM: "Vision impairment, progressive (onset in late childhood, teens)" [OMIM:Vision impairment, progressive (onset in late childhood, teens)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
X-linked Charcot-Marie-Tooth disease type 5 (Orphanet:99014)