Previous history
Xanthoma
integer
Café-au-lait spots
integer
Other symptoms of NF1
integer
1° relatives with NF1
integer
Previous congenital bone marrow failure disorder
integer
Previous acquired bone marrow failure disorder
integer
Previous malignancy
integer
Previous chemo-radiotherapy (CT and/or RT)
integer
Mental retardation
integer
Birth weight < third percentile
integer
Height < third percentile (at diagnosis)
integer
Weight < third percentile (at diagnosis)
integer
Head circumference < third percentile (at diagnosis)
integer
Clinical evidence of PNH
integer
Hepatitis/Hepatopathy
integer
Patient is twin
integer
Congenital abnormalities
integer
Other abnormalities
integer
Number of cafe au lait spots
Number of cafe au lait spots
integer
Type of other NF1 Symptoms
Neurofibromas of any type
integer
Plexiform neurofibroma
integer
Freckling in the axillary or inguinal regions
integer
Optic glioma
integer
>= 2 Lisch nodules of the iris
integer
Osseous lesions associated with NF1
integer
Degree of relationship of NF1 relatives
Type of previous cBMF
Previous congenital bone marrow failure disorder
integer
Type
text
Date and type of acquired BMF
Date and type of previous malignancy
Date of previous malignancy
date
Type of previous malignancy
integer
Other type of previous malignancy
text
Type of previous chemo therapy
Type of cong. abnormalities
Type of other abnormalties
Type of twin
Family history
Parents are consanguineous
integer
History of malignancies in family (1° relatives)
integer
History of Hemato-/ Immunological diseases
integer
History of other possibly relevant diseases
integer
Family history of malignancies
Mother affected
Father affected
Sister affected
Brother affected
Hemato/Immunological diseases in the family
Type of other diseases in the family