|
amorph type rh-null disease
|
C566210 |
|
|
peritoneal fibrosing syndromes
|
D056627 |
|
|
dysbetalipoproteinemia due to defect in apolipoprotein E-d
|
C566261 |
|
|
large-intestinal infection with Balantidium coli
|
5662 |
|
|
ovalocytosis, malaysian-melanesian-filipino type
|
C566230 |
|
|
spinal arterial venous malformations with cutaneous hemangiomas
|
C566282 |
|
|
ataxia, spastic, with congenital miosis
|
C566247 |
|
|
bilateral, with ureteral triplication and dysmorphism amastia
|
C566295 |
|
|
axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
|
C566234 |
|
|
familial granulomatous, with juvenile polyarthritis arteritis
|
C566253 |
|
|
hypomaturation-hypoplastic type, with taurodontism amelogenesis imperfecta
|
C566293 |
|
