class Information
has_dbxref
notation
Category
class Relations
Related from
part of
- Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome
- Legius syndrome
- Familial isolated café-au-lait macules
- Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome
- Gastrocutaneous syndrome
- Phakomatosis pigmentovascularis
- Naegeli-Franceschetti-Jadassohn syndrome
- Terminal osseous dysplasia-pigmentary defects syndrome
- Carney complex-trismus-pseudocamptodactyly syndrome
- Neuroectodermal melanolysosomal disease
- Osteopathia striata-pigmentary dermopathy-white forelock syndrome
- Familial progressive hyperpigmentation
- Fanconi anemia
- Peutz-Jeghers syndrome
- Intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome
- McCune-Albright syndrome
- Moynahan syndrome
- Hyperkeratosis-hyperpigmentation syndrome
- Dowling-Degos disease
- Dyschromatosis symmetrica hereditaria
- Dermatopathia pigmentosa reticularis
- Carney complex
- Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome
- Familial generalized lentiginosis
- Dyschromatosis universalis hereditaria
- Neurofibromatosis type 1
- Full schwannomatosis
- Dyskeratosis congenita
- Reticulate acropigmentation of Kitamura
- Mosaic Legius syndrome
- Noonan syndrome with multiple lentigines
- H syndrome
- X-linked reticulate pigmentary disorder
- Linear and whorled nevoid hypermelanosis
- Neurofibromatosis-Noonan syndrome