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hypohidrosis
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DOID_11155 |
[A sweat gland disease that is characterized by reduced ability to sweat, has_symptom hyperthermia and dry skin of affected areas, and has_material_basis_in trauma to the sweat glands.] |
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chief cell of parathyroid gland
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CL_0000446 |
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band keratopathy
|
DOID_11164 |
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Charcot-Marie-Tooth disease dominant intermediate B
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DOID_0110197 |
[A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in mutation in the gene encoding dynamin-2 (DNM2).] |
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common wart
|
DOID_11165 |
[A viral infectious disease that results_in infection located_in skin, has_material_basis_in human papillomavirus (types 2 and 4). This infection is characterized by a raised wart with roughened surface, most common on hands, but can grow anywhere on the body.] |
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anterior spinal artery
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UBERON_0005431 |
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Charcot-Marie-Tooth disease recessive intermediate C
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DOID_0110198 |
[A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in homozygous or compound heterozygous mutation in the PLEKHG5 gene on chromosome 1p36.] |
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Charcot-Marie-Tooth disease type 4E
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DOID_0110195 |
[A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or heterozygous mutation in the EGR2 gene on chromosome 10q21 or by heterozygous mutation in the MPZ gene on chromosome 1q23.] |
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obsolete apnea of prematurity
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DOID_11163 |
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Charcot-Marie-Tooth disease type 4G
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DOID_0110196 |
[A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22.] |
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Charcot-Marie-Tooth disease type 4F
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DOID_0110193 |
[A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the periaxin gene (PRX) on chromosome 19q13.] |
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neonatal respiratory failure
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DOID_11161 |
[A respiratory failure that is characterized by inadequate gas exchange by the respiratory system in neonates.] |
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Vagus nerve disease
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DOID_12491 |
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Charcot-Marie-Tooth disease type 4B3
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DOID_0110194 |
[A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the SBF1 gene on chromosome 22q.] |
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Charcot-Marie-Tooth disease type 4B1
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DOID_0110191 |
[A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the gene encoding the myotubularin-related protein-2 (MTMR2).] |
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Langerhans cell
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CL_0000453 |
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Charcot-Marie-Tooth disease type 4H
|
DOID_0110192 |
[A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutations in the gene encoding frabin (FGD4).] |
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clivus of occipital bone
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UBERON_0004108 |
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anogenital venereal wart
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DOID_11168 |
[A viral infectious disease that results_in infection located_in skin of vagina, cervix, uterus, anus, penis, scrotum, mouth, or throat, has_material_basis_in human papillomaviruses (types 6 and 11), which are transmitted_by direct contact with the skin during oral, genital, or anal sex with an infected partner. The infection has_symptom anogenital warts.] |
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obsolete vaginal condylomata acuminata
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DOID_11169 |
[An anogenital venereal wart that results_in infection located_in mucosa of vagina, has_material_basis_in human papillomaviruses (types 6 and 11), which are transmitted_by direct sexual contact with the skin of an infected partner. The infection has_symptom vaginal warts.] |