LL3739-1
[NEI] Ophthalmologic disease related systemic find
- Answer list
- LL3739-1
- Answers
- 39
Answers
| Answer | Code | Score |
|---|---|---|
| None | LA137-2 | |
| Ataxia | LA24636-5 | |
| Autism | LA24638-1 | |
| Cardiac defect(s) | LA24650-6 | |
| Cleft lip or palate | LA24660-5 | |
| CSF protein (>100mg/dl) | LA24682-9 | |
| Decreased bone density | LA24691-0 | |
| Delayed motor milestones | LA24693-6 | |
| Dementia | LA20372-1 | |
| Pediatric: Developmental delay | LA22265-5 | |
| Diabetes mellitus | LA14291-1 | |
| Dystonia | LA24705-8 | |
| Esophageal defect(s) | LA24714-0 | |
| Facial weakness | LA24720-7 | |
| Gastrointestinal defect(s) | LA24730-6 | |
| Gastrointestinal symptoms, recurrent | LA24731-4 | |
| Genitourinary defect(s) | LA24733-0 | |
| Headache, recurrent | LA24741-3 | |
| Hearing defect(s) | LA24742-1 | |
| Hypotonia | LA24751-2 | |
| Intellectual disabilities | LA24759-5 | |
| Klippel-feil | LA24771-0 | |
| Learning disability | LA24778-5 | |
| Limb malformations | LA24785-0 | |
| Limb weakness | LA24786-8 | |
| Myoclonus | LA24801-5 | |
| Pigmentation of skin different from other family members | LA24851-0 | |
| Polydactyly (digit abnormalities) | LA25437-7 | |
| Renal defect(s) | LA24872-6 | |
| Renal tubular dysfunction (Fanconi type) | LA24873-4 | |
| Scoliosis | LA22278-8 | |
| Seizures (history of, or treated) | LA24892-4 | |
| Short stature | LA24894-0 | |
| Skeletal defect(s) | LA24895-7 | |
| Stroke-like episodes associated with seizures | LA24908-8 | |
| Teeth defect(s) | LA24922-9 | |
| Umbilical abnormalities | LA24936-9 | |
| Other | LA46-8 | |
| Unknown | LA4489-6 |
Used by 1 tests
| LOINC |
|---|
| 79760-5 |