|
HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN
|
http://purl.obolibrary.org/obo/MONDO_0020989 |
|
|
hereditary motor and sensory neuropathy IIB
|
C537989 |
|
|
periapical dental abscess
|
6989 |
|
|
hereditary motor and sensory neuropathy 2 b (HMSN 2 b)
|
C537989 |
|
|
postaxial polydactyly-dental and vertebral anomalies syndrome
|
9895 |
|
|
charcot-marie-tooth disease, axonal, type 2b
|
C537989 |
|
|
antineutrophil cytoplasmic antibody-negative pauci-immune glomerulonephritis
|
19989 |
|
|
alpha 1 antitrypsin deficiency
|
D019896 |
|
|
MULLERIAN duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies
|
10989 |
|
|
MULLERIAN duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies; MURCS
|
http://purl.obolibrary.org/obo/MONDO_0010989 |
|
|
Mullerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome
|
10989 |
|
|
Müllerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome
|
10989 |
|
|
histiocytoma, fibrous, benign
|
2989 |
|
|
autosomal recessive benign erythrocytosis
|
9892 |
|
