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Disease association ontology term - MONDO:0021635 - neurocristopathy

Term summary

ID
MONDO:0021635
Name
neurocristopathy
Ontology or CV name
Disease association
Definition
That disease that arises from defects in the development of tissues containing cells commonly derived from the embryonic neural crest cell lineage.

Parents

Annotation

Disease association

MONDO:0010621 - CHILD syndrome

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Genes:

MONDO:0958175 - craniofacial microsomia 1

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Genes:

MONDO:0044792 - large congenital melanocytic nevus

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Genes:

MONDO:0008097 - linear nevus sebaceous syndrome

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Genes:

MONDO:0009578 - neurocutaneous melanocytosis

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MONDO:0008093 - nevus, epidermal

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MONDO:0000448 - paraganglioma

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Genes:

MONDO:0008192 - pheochromocytoma/paraganglioma syndrome 1

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MONDO:0011121 - pheochromocytoma/paraganglioma syndrome 2

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MONDO:0011544 - pheochromocytoma/paraganglioma syndrome 3

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Genes:

MONDO:0007273 - pheochromocytoma/paraganglioma syndrome 4

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MONDO:0013602 - pheochromocytoma/paraganglioma syndrome 5

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MONDO:0032771 - pheochromocytoma/paraganglioma syndrome 7

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Genes:

MONDO:0009131 - Riley-Day syndrome

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Genes: