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Results: 1 to 20 of 84

Make selection to find tests for any of the checked conditions.[x]
ConditionsSynonyms
Aminoglycoside-induced deafness
  • DEAFNESS, STREPTOMYCIN-INDUCED
  • STREPTOMYCIN OTOTOXICITY
Aminoglycoside antibacterials response
  • Aminoglycoside response
Epidermolysis bullosa simplex 1A, generalized severe
  • Epidermolysis bullosa herpetiformis, Dowling-Meara
  • Epidermolysis bullosa simplex Dowling-Meara type
Epidermolysis bullosa simplex 1C, localized
  • Cockayne-Touraine type epidermolysis bullosa
  • EBS, acral form
  • Epidermolysis Bullosa Simplex, Weber-Cockayne Type
  • Epidermolysis bullosa of hands and feet
  • Epidermolysis bullosa simplex, Cockayne-Touraine type
  • Localized epidermolysis bullosa simplex
  • Weber-Cockayne Syndrome
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome
  • KID syndrome, autosomal dominant
  • Keratitis-ichthyosis-deafness syndrome, autosomal dominant
  • Senter syndrome
Mitochondrial non-syndromic sensorineural hearing loss
  • Deafness, nonsyndromic sensorineural, mitochondrial
  • MT-CO1-Related Hearing Loss and Deafness
  • MT-RNR1-Related Hearing Loss and Deafness
  • MT-TS1-Related Hearing Loss and Deafness
  • Nonsyndromic Hearing Loss and Deafness, Mitochondrial
Epidermolysis bullosa simplex 5B, with muscular dystrophy
  • EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY
  • Epidermolysa bullosa simplex and limb girdle muscular dystrophy
  • Epidermolysis bullosa simplex with muscular dystrophy
Epidermolysis bullosa simplex, Koebner type
  • EBS 2
  • Epidermolysis Bullosa Simplex, Other Generalized
  • Generalized EBS
Epidermolysis bullosa simplex with mottled pigmentation
  • EBS with mottled pigmentation
  • EPIDERMOLYSIS BULLOSA SIMPLEX 2F, WITH MOTTLED PIGMENTATION
  • SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES AND CHILDHOOD BLISTERING
  • Speckled hyperpigmentation, palmo-plantar punctate keratoses and childhood blistering
Palmoplantar keratoderma-deafness syndrome
  • Diffuse palmoplantar keratoderma with deafness (subtype)
  • Focal palmoplantar keratoderma with sensorineural deafness (subtype)
  • Hereditary palmoplantar keratoderma with deafness (subtype)
  • Keratoderma palmoplantar deafness
  • Keratoderma palmoplantar, with deafness
  • Palmoplantar keratoderma and sensorineural deafness
Glucocorticoid deficiency with achalasia
  • AAA syndrome
  • ACTH-resistant adrenal insufficiency, achalasia and alacrima
  • Achalasia alacrima syndrome
  • Achalasia-Addisonianism-Alacrima (Triple-A) Syndrome
  • Achalasia-Addisonianism-Alacrima Syndrome
  • Achalasia-addisonianism-alacrimia syndrome
  • Addisonian achalasia syndrome
  • Alacrima-achalasia-addisonianism
  • Alacrima-achalasia-adrenal insufficiency neurologic disorder
  • Allgrove syndrome
  • Glucocorticoid deficiency and achalasia
  • Hypoadrenalism with achalasia
  • Triple-A syndrome
Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis
  • Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis
  • Erythrokeratodermia-cardiomyopathy syndrome
Ichthyosis, hystrix-like, with hearing loss
  • HID SYNDROME
  • Hystrix-like ichthyosis with deafness
Keratosis palmoplantaris striata 2
  • KERATODERMA, PALMOPLANTAR, STRIATE FORM II
  • Keratosis palmoplantaris striata II
  • STRIATE PALMOPLANTAR KERATODERMA II
Acral peeling skin syndrome
  • Peeling skin syndrome 2
  • Peeling skin syndrome, acral type (subtype)
Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive
  • Epidermolysis bullosa simplex, autosomal recessive
Palmoplantar keratoderma, epidermolytic
  • Localized epidermolytic hyperkeratosis
Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
  • Epidermolysis bullosa simplex due to BP230 deficiency
  • Epidermolysis bullosa simplex, autosomal recessive 2
Epidermolytic hyperkeratosis 1
  • BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA
Epidermolytic ichthyosis
  • Bullous erythroderma ichthyosiformis congenita of Brocq
  • Bullous ichthyosiform erythroderma
  • Bullous ichthyosiform erythroderma congenita
  • Congenital bullous ichthyosiform erythroderma
  • Epidermolytic Hyperkeratosis
  • KRT1-Related Epidermolytic Hyperkeratosis
  • KRT10-Related Epidermolytic Hyperkeratosis

Results: 1 to 20 of 84

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