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Hirschsprung's disease
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DOID_10487 |
[A megacolon that is characterized by a blockage of the large intestine due to improper muscle movement in the bowel.] |
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esophageal atresia
|
DOID_10485 |
|
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childhood teratoma of the ovary
|
DOID_6230 |
[An ovarian germ cell teratoma that presents in childhood.] |
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ovarian germ cell teratoma
|
DOID_5567 |
|
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psoriasis
|
DOID_8893 |
[A skin disease that is characterized by patches of thick red skin and silvery scales.] |
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pityriasis rosea
|
DOID_8892 |
[A dermatitis that is characterized by an initial large round spot on the chest, abdomen, or back, often referred to as a herald patch, that is usually followed within a week by a distinctive pattern of similar but smaller papules on the torso, arms, and legs.] |
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ovarian biphasic or triphasic teratoma
|
DOID_6232 |
[An ovarian germ cell teratoma that is composed of tissues that originate from two or three of the following germ layers, endoderm, ectoderm, or mesoderm.] |
|
vulvar eccrine porocarcinoma
|
DOID_7565 |
[A vulva carcinoma that is characterized by heterogenous histology that includes squamous cells, mucinous cells, clear cells, pigmented cells, and spindle cells and derives_from eccrine sweat glands.] |
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eccrine porocarcinoma
|
DOID_7566 |
|
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gross hematuria
|
SYMP_0000851 |
[A hematuria that is characterized by the production of a visible redness in the urine.] |
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mitochondrial complex IV deficiency nuclear type 13
|
DOID_0080360 |
[A COX deficiency, infantile mitochondrial myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the COA6 gene on chromosome 1q42.] |
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COX deficiency, infantile mitochondrial myopathy
|
DOID_0050713 |
[A cytochrome-c oxidase deficiency disease characterized by myotonia, abnormalities of the heart and kidneys, and lactic acidosis.] |
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anuria
|
SYMP_0000852 |
[A urinary system symptom that is characterized by the absence of, or by defective, urine excretion.] |
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non-invasive bladder papillary urothelial neoplasm
|
DOID_6239 |
|
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trimethylaminuria
|
DOID_0080361 |
[An inherited metabolic disorder characterized by the inability to break down trimethylamine and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding flavin-containing monooxygenase-3 on chromosome 1q24.] |
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vulvar clear cell hidradenocarcinoma
|
DOID_7567 |
[A vulva carcinoma that derives_from sweat glands and is characterized by the presence of clear cells.] |
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X-linked spondyloepiphyseal dysplasia tarda
|
DOID_0080362 |
[A spondyloepiphyseal dysplasia that is characterized by impaired growth of bones of the spine and the ends of long bones in the arms and legs and has_material_basis_in mutation in the SEDL gene on chromosome Xp22.] |
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spondyloepiphyseal dysplasia tarda
|
DOID_0112284 |
[A spondyloepiphyseal dysplasia characterized by impaired growth of the bones of the spine and the ends of the long bones that becomes apparent in after birth.] |
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congested sclera
|
SYMP_0000850 |
[Congested sclera is a hyperemia characterized as the congestion of the vessels of the outer layer of the eye containing collagen and elastic fibers.] |
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obsolete adult brain meningioma
|
DOID_7568 |
|