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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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RETICULAR DYSGENESIA
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C0272167 |
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RETICULAR DYSGENESIS
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C0272167 |
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Reticular Dysgenesis
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C0272167 |
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Reticular dysgenesia
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C0272167 |
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Reticular dysgenesis
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C0272167 |
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congenital Aleukia
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C0272167 |
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congenital aleukocytosis
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C0272167 |
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reticular Dysgenesia
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C0272167 |
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reticular dysgenesis
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C0272167 |
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DE VAAL DISEASE
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C0272167 |
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Generalized hematopoietic hypoplasia
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C0272167 |
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De Vaal disease
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C0272167 |
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SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia
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C0272167 |
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haematopoietic hypoplasia, generalised
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C0272167 |
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hematopoietic hypoplasia, generalized
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C0272167 |
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