Genetic disorders with no OMIM
- 2q37 deletion syndrome
- 8p23.1 duplication syndrome
- Acytosiosis
- Amelanism
- Aniridia renal agenesis psychomotor retardation
- Axanthism
- Banti's syndrome
- Bare lymphocyte syndrome type II
- Chromosome 15q partial deletion
- Chromosome 15q trisomy
- Congenital dyserythropoietic anemia
- Congenital dyserythropoietic anemia type I
- Congenital dyserythropoietic anemia type II
- Congenital dyserythropoietic anemia type III
- Congenital dyserythropoietic anemia type IV
- Congenital fibrosis of the extraocular muscles
- Cooks syndrome
- Distal trisomy 10q
- Erondu–Cymet syndrome
- Erythrism
- Fibrous dysplasia of bone
- Frontotemporal dementia and parkinsonism linked to chromosome 17
- GMS syndrome
- Hemoglobin variants
- Hereditary spastic paraplegia
- Interleukin-1 receptor–associated kinase 4 deficiency
- Isodicentric 15
- Lachiewicz–Sibley syndrome
- Lethal arthrogryposis with anterior horn cell disease
- Lethal white syndrome
- Leucism
- Melanism
- Monostotic fibrous dysplasia
- Nullisomic
- Partial monosomy 13q
- Ring chromosome 20 syndrome
- Scott syndrome
- Singleton Merten syndrome
- Snatiation
- Tetrasomy 18p
- Tetrasomy 9p
- Xanthochromism
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Genetic disorders with no OMIM
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