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obsolete Diabetes mellitus of mother, with delivery
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DOID_12584 |
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velocardiofacial syndrome
|
DOID_12583 |
[A chromosomal deletion disease that has_material_basis_in da 1.5- to 3.0-Mb hemizygous deletion of chromosome 22q11.2 and that is characterized by variable developmental problems and schizoid features. Haploinsufficiency of the TBX1 gene in particular is responsible for most of the physical malformations.] |
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obsolete enthesopathy of elbow
|
DOID_12582 |
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rosacea conjunctivitis
|
DOID_9709 |
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olecranon bursitis
|
DOID_12581 |
[A bursitis that is characterized by an inflammation of the bursa, located at the tip of the elbow (olecranon process).] |
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Cri-Du-Chat syndrome
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DOID_12580 |
[A syndrome that has_material_basis_in deletion of the end of the chromosome 5 p arm and that is characterized by intellectual disability, delayed development, small head size, low birth weight, weak muscle tone widely set eyes, low-set ears, a small jaw, a rounded face and a high-pitched cry that sounds like that of a cat.] |
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haploid cell
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CL_0000413 |
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adrenal/interrenal gland
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UBERON_0006858 |
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cat-scratch disease
|
DOID_11258 |
[A bartonellosis that results_in infection located_in lymph node, has_material_basis_in Bartonella henselae or has_material_basis_in Bartonella clarridgeiae, which are transmitted_by scratch or bite of a kitten, or transmitted_by contact of animal's saliva with an eye or through broken skin. The infection has_symptom regional lymphadenopathy, has_symptom headache, has_symptom chills, has_symptom backache, and has_symptom abdominal pain.] |
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obsolete Cytomegalovirus infectious disease
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DOID_11259 |
[A viral infectious disease that results_in infection in animals and humans, has_material_basis_in Cytomegalovirus, which is transmitted_by contact with the infected person's bodily fluids or transmitted_by sexual contact, or transmitted_by blood transfusions.] |
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social phobia
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DOID_11257 |
[A phobic disorder that involves social anxiety occurring only in specific public or social situations, interactions with others or being evaluated or scrutinized by other people.] |
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phobic disorder
|
DOID_591 |
[An anxiety disorder where fear and anxiety are triggered by a specific stimulus or situation.] |
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Brill-Zinsser disease
|
DOID_11254 |
[An epidemic typhus that is a mild form of the disease, which recurs in someone after a long period of latency due to immunosuppression, malnutrition or other illnesses.] |
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epidemic typhus
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DOID_0050480 |
[A typhus that has_material_basis_in Rickettsia prowazekii, which is transmitted by human body louse (Pediculus humanus corporis). The infection has_symptom high fever, has_symptom cough, has_symptom rash, has_symptom severe muscle pain, has_symptom chills, has_symptom falling blood pressure, has_symptom stupor, has_symptom sensitivity to light, and has_symptom delirium.] |
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bacterial conjunctivitis
|
DOID_9700 |
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chlamydia
|
DOID_11263 |
[A commensal bacterial infectious disease that is caused by Chlamydia trachomatis.] |
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autosomal recessive limb-girdle muscular dystrophy type 2M
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DOID_0110296 |
[An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding fukutin (FKTN) on chromosome 9q31.] |
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Potter's syndrome
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DOID_12594 |
[A renal agenesis characterized by the typical physical appearance and associated pulmonary hypoplasia of a newborn as a direct result of kidney failure, oligohydramnios and compression while in the uterus.] |
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obsolete Chlamydophila infectious disease
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DOID_11264 |
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autosomal recessive limb-girdle muscular dystrophy type 2K
|
DOID_0110297 |
[An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding protein O-mannosyltransferase (POMT1).] |