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Items: 5

1.

Laurin-Sandrow syndrome

Laurin-Sandrow syndrome (LSS) is an autosomal dominant disorder characterized by polysyndactyly of hands and feet, mirror image duplication of feet, and nasal defects (hypoplastic alae nasi, short columella), in connection with absent patella and duplicated fibula (summary by Lohan et al., 2014). [from OMIM]

MedGen UID:
340697
Concept ID:
C1851100
Disease or Syndrome
2.

Hypoglossal nerve disorder

A non-neoplastic or neoplastic disorder affecting the hypoglossal nerve (twelfth cranial nerve). [from NCI]

MedGen UID:
57513
Concept ID:
C0152181
Disease or Syndrome
3.

Neurodegeneration

Progressive loss of neural cells and tissue. [from HPO]

MedGen UID:
17999
Concept ID:
C0027746
Cell or Molecular Dysfunction
4.

Cranial nerve neuropathy

A neoplastic or non-neoplastic disorder that affects one of the cranial nerves. [from NCI]

MedGen UID:
1160
Concept ID:
C0010266
Disease or Syndrome
5.

Hypoglossal nerve neoplasm

A neoplasm involving a hypoglossal nerve. [from MONDO]

MedGen UID:
220392
Concept ID:
C1263903
Neoplastic Process
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