|
obsolete mixed disorder as reaction to stress
|
DOID_12379 |
|
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obsolete predominant psychomotor disturbance
|
DOID_12378 |
|
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Fungi incertae sedis
|
NCBITaxon_112252 |
|
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Leber congenital amaurosis 1
|
DOID_0110078 |
[A Leber congenital amaurosis characterized by severe cone-rod dystrophy with photophobia, high hyperopia, and poor but stable vision with no visual improvement and that has_material_basis_in mutation in the GUCY2D gene on chromosome 17p13.] |
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juvenile spinal muscular atrophy
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DOID_12376 |
[A childhood spinal muscular atrophy that has age of onset after 18 months and is characterized by muscle weakness after early childhood and the ability to stand and walk and that has_material_basis_in homozygous or compound heterozygous mutation in the SMN1 gene on chromosome 5q13.] |
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Leber congenital amaurosis 8
|
DOID_0110079 |
[A Leber congenital amaurosis that is characterized by night blindness and thick unlaminated retinas and has_material_basis_in mutation in the CRB1 gene on chromosome 1q31-q32.] |
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Waterhouse-Friderichsen syndrome
|
DOID_9931 |
[An adrenal gland disease that is characterized by failure of the adrenal gland due to bleeding into the gland.] |
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obsolete primary Neisseriaceae infectious disease
|
DOID_9930 |
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obsolete carcinoid syndrome
|
DOID_8600 |
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chronic inflammation of lacrimal passage
|
DOID_9935 |
[A lacrimal apparatus disease that is characterized by longstanding inflammation of the lacrimal passage, and has_symptom pain, increased or decreased tearing, and swelling between the eye and nose.] |
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obsolete Hodgkin's lymphoma, lymphocytic-histiocytic predominance involving intrapelvic lymph nodes
|
DOID_8604 |
|
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Leber congenital amaurosis 12
|
DOID_0110080 |
[A Leber congenital amaurosis that has_material_basis_in mutation in the RD3 gene on chromosome 1q32.] |
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upper gum cancer
|
DOID_8601 |
|
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gum cancer
|
DOID_8602 |
|
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herpetic whitlow
|
DOID_8607 |
[A herpes simplex that results_in infection located_in skin of the finger, toe, or thumb, has_material_basis_in Human herpesvirus 1 (Simplexvirus humanalpha1) or 2 (Simplexvirus humanalpha2) and has_symptom lesions, has_symptom fever, and has_symptom swollen lymph nodes.] |
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dacryocystocele
|
DOID_9939 |
|
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chronic dacryocystitis
|
DOID_9937 |
|
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chronic canaliculitis
|
DOID_9936 |
|
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chest wall
|
UBERON_0016435 |
|
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balantidiasis
|
DOID_12386 |
[A parasitic protozoa infectious disease involving infection caused by Balantidium coli. The trophozoites are capable of attacking the intestinal epithelium, creating ulcers and causing bloody diarrhea. The infectiou has_symptom cramping, has_symptom abdominal pain, has_symptom nausea and has_symptom foul breath.] |