Diamond-Blackfan anemia 7
- Synonyms
- RPL11-Related Diamond-Blackfan Anemia
Summary
Excerpted from the GeneReview:- Full text of GeneReview (by section):
- Summary
- Diagnosis
- Clinical Characteristics
- Genetically Related (Allelic) Disorders
- Differential Diagnosis
- Management
- Genetic Counseling
- Resources
- Molecular Genetics
- Chapter Notes
- References
- Authors:
- Colin Sieff
- view full author information
Available tests
Check Related conditions for additional relevant tests.
Clinical tests (51 available)
Clinical features
Help- Abnormality of blood and blood-forming tissues
- Increased mean corpuscular volume
Increased mean corpuscular volume
- MedGen UID: 81303
- Concept ID: C0302845
- Finding: Finding
Abnormality of blood and blood-forming tissues
- Macrocytic anemia
Macrocytic anemia
- MedGen UID: 1920
- Concept ID: C0002886
- Finding: Disease or Syndrome
Abnormality of blood and blood-forming tissues
- Increased mean corpuscular volume
- Abnormality of head or neck
- Choanal atresia
Choanal atresia
- MedGen UID: 3395
- Concept ID: C0008297
- Finding: Congenital Abnormality
Abnormality of head or neck
- Cleft palate
Cleft palate
- MedGen UID: 756015
- Concept ID: C2981150
- Finding: Congenital Abnormality
Abnormality of head or neck
- Choanal atresia
- Abnormality of limbs
- Short thumb
Short thumb
- MedGen UID: 98469
- Concept ID: C0431890
- Finding: Congenital Abnormality
Abnormality of limbs
- Small hypothenar eminence
Small hypothenar eminence
- MedGen UID: 396124
- Concept ID: C1861395
- Finding: Finding
Abnormality of limbs
- Triphalangeal thumb
Triphalangeal thumb
- MedGen UID: 66029
- Concept ID: C0241397
- Finding: Congenital Abnormality
Abnormality of limbs
- Short thumb
- Abnormality of metabolism/homeostasis
- Low levels of vitamin D
Low levels of vitamin D
- MedGen UID: 12114
- Concept ID: C0042870
- Finding: Disease or Syndrome
Abnormality of metabolism/homeostasis
- Low levels of vitamin D
- Abnormality of prenatal development or birth
- Fetal distress
Fetal distress
- MedGen UID: 5164
- Concept ID: C0015930
- Finding: Pathologic Function
Abnormality of prenatal development or birth
- Polyhydramnios
Polyhydramnios
- MedGen UID: 6936
- Concept ID: C0020224
- Finding: Pathologic Function
Abnormality of prenatal development or birth
- Fetal distress
- Abnormality of the cardiovascular system
- Patent ductus arteriosus
Patent ductus arteriosus
- MedGen UID: 4415
- Concept ID: C0013274
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Secundum atrial septal defect
Secundum atrial septal defect
- MedGen UID: 91034
- Concept ID: C0344724
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Tetralogy of Fallot
Tetralogy of Fallot
- MedGen UID: 21498
- Concept ID: C0039685
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Ventricular septal defect
Ventricular septal defect
- MedGen UID: 42366
- Concept ID: C0018818
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Patent ductus arteriosus
- Abnormality of the digestive system
- Esophagitis
Esophagitis
- MedGen UID: 4549
- Concept ID: C0014868
- Finding: Disease or Syndrome
Abnormality of the digestive system
- Esophagitis
- Abnormality of the ear
- Atresia of the external auditory canal
Atresia of the external auditory canal
- MedGen UID: 78613
- Concept ID: C0266597
- Finding: Congenital Abnormality
Abnormality of the ear
- Hearing impairment
Hearing impairment
- MedGen UID: 235586
- Concept ID: C1384666
- Finding: Disease or Syndrome
Abnormality of the ear
- Atresia of the external auditory canal
- Abnormality of the genitourinary system
- Horseshoe kidney
Horseshoe kidney
- MedGen UID: 65140
- Concept ID: C0221353
- Finding: Congenital Abnormality
Abnormality of the genitourinary system
- Vesicoureteral reflux
Vesicoureteral reflux
- MedGen UID: 21852
- Concept ID: C0042580
- Finding: Disease or Syndrome
Abnormality of the genitourinary system
- Horseshoe kidney
- Abnormality of the immune system
- Neutropenia
Neutropenia
- MedGen UID: 163121
- Concept ID: C0853697
- Finding: Finding
Abnormality of the immune system
- Recurrent infections
Recurrent infections
- MedGen UID: 65998
- Concept ID: C0239998
- Finding: Finding
Abnormality of the immune system
- Recurrent otitis media
Recurrent otitis media
- MedGen UID: 155436
- Concept ID: C0747085
- Finding: Disease or Syndrome
Abnormality of the immune system
- Neutropenia
- Abnormality of the musculoskeletal system
- Congenital elevation of scapula
Congenital elevation of scapula
- MedGen UID: 56291
- Concept ID: C0152438
- Finding: Congenital Abnormality
Abnormality of the musculoskeletal system
- Osteopenia
Osteopenia
- MedGen UID: 18222
- Concept ID: C0029453
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Osteoporosis
Osteoporosis
- MedGen UID: 14535
- Concept ID: C0029456
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Scoliosis
Scoliosis
- MedGen UID: 11348
- Concept ID: C0036439
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Congenital elevation of scapula
- Growth abnormality
- Fetal growth restriction
Fetal growth restriction
- MedGen UID: 4693
- Concept ID: C0015934
- Finding: Pathologic Function
Growth abnormality
- Growth delay
Growth delay
- MedGen UID: 99124
- Concept ID: C0456070
- Finding: Pathologic Function
Growth abnormality
- Fetal growth restriction
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.