brachial amelia, forebrain defects, and facial clefts
|
C536713 |
|
iranian variant form mucolipidosis III
|
C565367 |
|
anemia, sex-linked hypochromic sideroblastic
|
C536761 |
|
yemenite deaf-blind hypopigmentation syndrome
|
C536771 |
|
white matter hypoplasia, corpus callosum agenesia, and mental retardation
|
C536701 |
|
woolly hair, hypotrichosis, everted lower lip and outstanding ears
|
C536746 |
|
woolly hair, hypotrichosis, everted lower lip, and outstanding ears
|
C536746 |
|
azoospermia sinopulmonary infections
|
C536718 |
|
zadik barak levin syndrome
|
C536721 |
|
primary t-cell immunodeficiency disorders
|
C536780 |
|
t cell immunodeficiency primary
|
C536780 |
|
winship viljoen leary syndrome
|
C536711 |
|
mucolipidosis III, iranian variant form
|
C565367 |
|
encephalopathy, fatal infantile, with olivopontocerebellar hypoplasia
|
C536716 |
|