neurocristopathy
MONDO:0021635Mondo
Findings
No curated finding names neurocristopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
That disease that arises from defects in the development of tissues containing cells commonly derived from the embryonic neural crest cell lineage.
Definition from the Mondo Disease Ontology (MONDO:0021635), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (16)
- Axenfeld-Rieger syndrome
- central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease
- CHARGE syndrome
- craniofacial microsomia
- craniofrontonasal syndrome
- cutaneous neuroendocrine carcinoma
- DiGeorge syndrome
- Hirschsprung disease
- melanocytic neoplasm
- multiple endocrine neoplasia
- neuroblastoma
- neurofibromatosis type 1
- paraganglioma
- piebaldism
- Riley-Day syndrome
- Waardenburg-Shah syndrome
Other names
3 names
Resolves to: neurocristopathy
- Also called
- disorder of neural crest cell developmentdisorder of neural crest developmentneural crest cell development disease