The following pages link to 1q21.1 deletion syndrome
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Jacobsen syndrome (links | edit)
- Smith–Lemli–Opitz syndrome (links | edit)
- Haploinsufficiency (links | edit)
- Small supernumerary marker chromosome (links | edit)
- Saethre–Chotzen syndrome (links | edit)
- Desmoplastic small-round-cell tumor (links | edit)
- Ring chromosome (links | edit)
- Smith–Magenis syndrome (links | edit)
- CHARGE syndrome (links | edit)
- Trisomy 8 (links | edit)
- Fraser syndrome (links | edit)
- VACTERL association (links | edit)
- Carpenter syndrome (links | edit)
- Trisomy 9 (links | edit)
- Polysomy (links | edit)
- Y chromosome microdeletion (links | edit)
- Follicular lymphoma (links | edit)
- Goldenhar syndrome (links | edit)
- Neuroacanthocytosis (links | edit)
- Chromosome 1 (links | edit)
- Pfeiffer syndrome (links | edit)
- Asymmetric crying facies (links | edit)
- Fountain syndrome (links | edit)
- List of ICD-9 codes 740–759: congenital anomalies (links | edit)
- XX male syndrome (links | edit)
- Caudal regression syndrome (links | edit)
- Bannayan–Riley–Ruvalcaba syndrome (links | edit)
- Seckel syndrome (links | edit)
- XXYY syndrome (links | edit)
- Laurence–Moon syndrome (links | edit)
- Robinow syndrome (links | edit)
- Monosomy 9p (links | edit)
- Primordial dwarfism (links | edit)
- Pallister–Killian syndrome (links | edit)
- Holt–Oram syndrome (links | edit)
- XXXXY syndrome (links | edit)
- Nail–patella syndrome (links | edit)
- Diffuse large B-cell lymphoma (links | edit)
- XX gonadal dysgenesis (links | edit)
- Gonadal dysgenesis (links | edit)
- Catel–Manzke syndrome (links | edit)
- Pierre Robin sequence (links | edit)
- 22q13 deletion syndrome (links | edit)
- Acrocephalosyndactyly (links | edit)
- Chromosome abnormality (links | edit)
- Ectromelia (links | edit)
- Olduvai domain (links | edit)
- Hemojuvelin (links | edit)
- Ring chromosome 20 syndrome (links | edit)
- Hemimegalencephaly (links | edit)