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Timothy Syndrome
Timothy syndrome
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Related in the Kosmos
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Channelopathy
(42)
Andersen syndrome
Brugada syndrome
Long qt syndrome
Romano-ward syndrome
Achromatopsia
Achromatopsia
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal dominant polycystic kidney
Bartter syndrome
Benign familial neonatal convulsions
Calciumopathy
Channelome
Childhood absence epilepsy
Congenital hyperinsulinism
Congenital insensitivity to pain
Cystic fibrosis
Episodic ataxia
Erythromelalgia
Familial atrial fibrillation
Familial hemiplegic migraine
Focal segmental glomerulosclerosis
Generalized epilepsy with febrile seizures plus
Hyperkalemic periodic paralysis
Hypokalemic periodic paralysis
Hypokalemic sensory overstimulation
Hypomagnesemia with secondary hypocalcemia
Juvenile myoclonic epilepsy
Maculopathy
Malignant hyperthermia
Mucolipidosis type IV
Myotonia congenita
Nonsyndromic deafness
Paramyotonia congenita
Paroxysmal extreme pain disorder
Periodic paralysis
Potassium-- aggravated myotonia
Pseudohypo- aldosteronism
Retinitis pigmentosa
Rolandic epilepsy
Short QT syndrome
Spinocerebellar ataxia type-13
Spinocerebellar ataxia type-6
X-linked congenital stationary night blindness
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Genetic disorders
(39)
Adducted thumb syndrome
Sakati-Nyh- an-Tisdale syndrome
Urban Rogers Meyer syndrome
Acrocephal- osyndactylia
Genodermatoses
Genodermatoses
Zimmerman Laband syndrome
Aarskog-Scott syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Lelis syndrome
Familial cutaneous papillomatosis
Yunis Varon syndrome
Eem syndrome
Donohue syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Branchio-Oto-Renal Syndrome
Ichthyosis lamellaris
Laurence Moon syndrome
Apert syndrome
Bardet Biedl Syndrome
Adrenoleuk- odystrophy
Sabinas brittle hair syndrome
DNA repair-deficiency disorder
Carpenter syndrome
Congenital ichthyosiform erythroderma
Beckwith wiedemann syndrome
Glycogen storage disease type iib
Abdallat Davis Farrage syndrome
Dermatopathia pigmentosa reticularis
Kindler syndrome
Vacterl association
Thymic aplasia
Jervell and Lange-Nielsen syndrome
Long qt syndrome
Brugada syndrome
Andersen syndrome
Romano-ward syndrome
more...
Medical condition
(37)
Meleda Disease
Acanthosis nigricans
Syndactyly
Trichilemmal cyst
Ectodermal dysplasia
Ectodermal dysplasia
Actinic keratosis
Pili annulati
Pemphigus vulgaris
Acute lymphadenitis
Cardiac arrhythmia
Pemphigoid, bullous
Uncombable hair syndrome
Adducted thumb syndrome
Sakati-Nyh- an-Tisdale syndrome
Acrocephal- osyndactylia
Aarskog-Scott syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Eem syndrome
Donohue syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Long qt syndrome
Branchio-Oto-Renal Syndrome
Ichthyosis lamellaris
Apert syndrome
Bardet Biedl Syndrome
Sabinas brittle hair syndrome
Carpenter syndrome
Brugada syndrome
Beckwith wiedemann syndrome
Glycogen storage disease type iib
Dermatopathia pigmentosa reticularis
Vacterl association
Thymic aplasia
Romano-ward syndrome
more...
Autosomal recessive disorders
(18)
Adducted thumb syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Yunis Varon syndrome
Eem syndrome
Donohue syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Sabinas brittle hair syndrome
Carpenter syndrome
Congenital ichthyosiform erythroderma
Glycogen storage disease type iib
Abdallat Davis Farrage syndrome
Kindler syndrome
Jervell and Lange-Nielsen syndrome
more...
Genetic disorder
(12)
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Branchio-Oto-Renal Syndrome
Laurence Moon syndrome
Sabinas brittle hair syndrome
Abdallat Davis Farrage syndrome
more...
Cutaneous conditions
(41)
Conditions of the skin appendages
Disturbances of human pigmentation
Endocrine-related skin conditions
Epidermal nevi, neoplasms, cysts
Papulosquamous hyperkeratotic skin diseases
Papulosquamous hyperkeratotic skin diseases
Acne-related skin conditions
Acneiform eruptions
Autoinflammatory syndromes
Chronic blistering cutaneous conditions
Conditions of the mucous membranes
Conditions of the subcutaneous fat
Connective tissue diseases
Dermal and subcutaneous growths
Dermatitis
Drug eruptions
Endocrine-related cutaneous conditions
Erythemas
Genodermatoses
Infection-related cutaneous conditions
Lichenoid eruptions
List of cutaneous conditions
Lymphoid-related cutaneous conditions
Lymphoid-related skin conditions
Melanocytic nevi and neoplasms
Monocyte and macrophage-related skin conditions
Monocyte- and macrophage-related cutaneous conditions
Mucinoses
Neurocutaneous conditions
Noninfectious immunodefi- ciency-related cutaneous conditions
Noninfectious immunodefi- ciency-related skin conditions
Pruritic skin conditions
Psoriasis
Reactive neutrophilic cutaneous conditions
Reactive neutrophilic skin conditions
Recalcitrant palmoplantar eruptions
Skin conditions resulting from errors in metabolism
Skin conditions resulting from physical factors
Skin disease
Urticaria and angioedema
Vascular skin conditions
Vascular-related cutaneous conditions
more...
Dermatology
(15)
Acral Acanthotic Anomaly
Acne aestivalis
Onychauxis
Sign of Leser-Trelat
Anonychia
Anonychia
Skin appendages
Bacterial skin disease
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Lelis syndrome
Familial cutaneous papillomatosis
Meleda Disease
Pili annulati
Pemphigus vulgaris
Pemphigoid, bullous
more...
Ion channels
(8)
CACNA1c
Calcium channel
MiRP1
KvLQT1
Sodium channel
Sodium channel
Potassium channel
SCN5A
KCNJ2
more...
Diseases and disorders
(11)
Keratin disease
Weaver syndrome
Acneiform eruption
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Yunis Varon syndrome
Abdallat Davis Farrage syndrome
Chromhidrosis
Ectodermal dysplasia
Dermatopathia pigmentosa reticularis
Vacterl association
more...
See also
(20)
William Berger (author)
Nevus flammeus nuchae
Subcutaneous tissue
Integument
Congenital malformations
Congenital malformations
Silver-Russell dwarfism
Autosomal dominant
Autosomal recessive
Skin lesion
Autosomal
Repolarization
Florid cutaneous papillomatosis
Qt interval
Elston
Diseases Database
Acrodermatitis Chronica Atrophicans
Chromhidrosis
People
People associated with religion
Hyper IgM Syndrome Type 1
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