Rare – Page 314 – CheckOrphan

Common variable immunodeficiency

[...]

Complement component deficiency

[...]

Hereditary fructose intolerance

[...]

Craniosynostosis- anal anomalies- and porokeratosis

[...]

Craniosynostosis Warman type

[...]

Craniosynostosis Fontaine type

[...]

Peptidic growth factors deficiency

[...]

Craniosynostosis mental retardation clefting syndrome

[...]

Craniosynostosis Maroteaux Fonfria type

[...]

Brachydactylous dwarfism Mseleni type

[...]