Disease Browser
|
Parent Node: Congenital Microtia (D065817) | Parent Node: Hearing Loss, Conductive (D006314) | Parent Node: Mastocytosis, Cutaneous (D034701) | ..Starting node ..Mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia (C536033)
| Child Nodes:
|
Sister Nodes: | ..Mastocytoma, Skin (D054705)
| ..Mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia (C536033)
| ..Urticaria Pigmentosa (D014582)
|
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
|
|
|
Term ID: | 6825 |
Name: | Mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D006314|MESH:D034701|MESH:D065817 |
TreeNumbers: | C04.557.450.565.465.500/C536033 |C09.218.235/C536033 |C09.218.458.341.562/C536033 |C10.597.751.418.341.562/C536033 |C16.131.287/C536033 |C17.800.508.473/C536033 |C23.888.592.763.393.341.562/C536033 |
Synonyms: | |
Slim Mappings: | Cancer|Congenital abnormality|Ear-nose-throat disease|Nervous system disease|Signs and symptoms|Skin disease |
Reference: |
MedGen: C536033
MeSH: C536033
OMIM: 248910;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
|