|
obsolete metastatic melanoma
|
DOID_4358 |
|
|
obsolete experimental melanoma
|
DOID_4357 |
|
|
Werner syndrome
|
DOID_5688 |
[A progeroid syndrome characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers and that has_material_basis_in mutations in the WRN gene, on chromosome 8.] |
|
obsolete metastatic adenocarcinoma
|
DOID_3027 |
|
|
obsolete intramucosal adenocarcinoma colon adenoma
|
DOID_3028 |
|
|
Hexamitidae
|
NCBITaxon_5739 |
|
|
Diplomonadida
|
NCBITaxon_5738 |
|
|
amelanotic melanoma
|
DOID_4359 |
|
|
colon mucinous adenocarcinoma
|
DOID_3029 |
|
|
colon adenocarcinoma
|
DOID_234 |
[A colon carcinoma that derives_from epithelial cells of glandular origin.] |
|
mucinous adenocarcinoma
|
DOID_3030 |
[An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which produce mucin.] |
|
Fornicata
|
NCBITaxon_207245 |
|
|
congenital disorder of deglycosylation 1
|
DOID_0060728 |
[A carbohydrate metabolic disorder that is characterized by global developmental delay, hypotonia, abnormal involuntary movements, and alacrima or poor tear production and that has_material_basis_in homozygous or compound heterozygous mutation in the NGLY1 gene on chromosome 3p24.] |
|
congenital disorder of deglycosylation
|
DOID_0060991 |
[A carbohydrate metabolic disorder that is charactized mutations resulting in malfunction impacting the addition of glycans to proteins.] |
|
Language impairment
|
HP_0002463 |
|
|
Abnormal communication
|
HP_0034434 |
|
|
Acanthomorphata
|
NCBITaxon_123368 |
|
|
autosomal recessive congenital ichthyosis 11
|
DOID_0060720 |
[An autosomal recessive congenital ichthyosis characterized by ichthyosis, hypotrichosis, photophobia, corneal opacity, pingueculum, blepharitis, marked acanthosis, otrhohyperkeratosis and hyperkeratosis that has_material_basis_in homozygous mutation in the ST14 gene on chromosome 11q24.] |
|
cellular myxoid liposarcoma
|
DOID_5692 |
|
|
visual cortex disease
|
DOID_5691 |
|