|
rare coagulopathy due to a constitutional thrombopathy and/or thrombocytopenia
|
http://purl.obolibrary.org/obo/MONDO_0019097 |
|
|
BCG infection, generalized familial semibenign, autosomal dominant
|
C565909 |
|
|
skeletal defects, genital hypoplasia, and intellectual disability
|
12909 |
|
|
skeletal defects, genital hypoplasia, and mental retardation
|
12909 |
|
|
major vestibular gland adenomyoma
|
3909 |
|
|
nephrogenic diabetes insipidus-intracranial calcification syndrome
|
9099 |
|
|
leukoencephalopathy, diffuse hereditary, with spheroids
|
9096 |
|
|
leukoencephalopathy, diffuse hereditary, with spheroids; HDLS
|
http://purl.obolibrary.org/obo/MONDO_0009096 |
|
|
pseudocorpus luteum insufficiency
|
9909 |
|
|
syndromic X-linked intellectual disability Hough type
|
30909 |
|
|
autosomal dominant intermediate Charcot-Marie-Tooth disease type D
|
11909 |
|
