|
familial lupus anticoagulant
|
C531622 |
|
|
unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemia
|
43168 |
|
|
familial spinal arachnoiditis
|
C531624 |
|
|
spinal tuberculous arachnoiditis
|
C531624 |
|
|
physiological malfunction arising from mental Factor
|
24316 |
|
|
nephronophthisis (disease) caused by mutation in XPNPEP3
|
13163 |
|
|
astrocytoma of cerebellum
|
3165 |
|
|
autosomal recessive complex spastic paraplegia caused by mutation in NT5C2
|
13165 |
|
|
acantholytic squamous cell carcinoma of skin
|
4316 |
|
|
acantholytic squamous cell carcinoma of the skin
|
4316 |
|
|
acantholytic squamous cell skin carcinoma
|
4316 |
|
|
monosomy 2q24 chromosome 2
|
C538316 |
|
