|
non-syndromic polydactyly, syndactyly and/or hyperphalangy
|
19714.0 |
|
|
mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy
|
20714.0 |
|
|
progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
|
14714.0 |
|
|
primary intralymphatic angioendothelioma
|
18714.0 |
|
|
bladder urachal squamous cell carcinoma
|
3714.0 |
|
|
atrophic muscular disease
|
4714.0 |
|
|
Pelizaeus-Merzbacher disease
|
10714.0 |
|
|
acyl-CoA dehydrogenase deficiency
|
17714.0 |
|
|
tumoral calcinosis, hyperphosphatemic, familial, 2
|
60714.0 |
|
|
obsolete migraine, familial hemiplegic, 1
|
7714.0 |
|
|
mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
|
44714.0 |
|
|
central nervous system cancer
|
2714.0 |
|
|
mannose-binding lectin deficiency
|
13714.0 |
|
