ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Phakomatosis

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Phakomatosis

ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities vs. Phakomatosis

ICD-10 is an international statistical classification used in health care and related industries. Phakomatoses refers to a group of neuro-oculo-cutaneous syndromes or neurocutaneous disorders involving structures arising from the embryonic ectoderm.

Similarities between ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Phakomatosis

ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Phakomatosis have 5 things in common (in Unionpedia): Incontinentia pigmenti, Neurofibromatosis, Sturge–Weber syndrome, Tuberous sclerosis, Von Hippel–Lindau disease.

Incontinentia pigmenti

Incontinentia pigmenti (IP) is a rare genetic disorder that affects the skin, hair, teeth, nails, and central nervous system.

ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Incontinentia pigmenti · Incontinentia pigmenti and Phakomatosis · See more »

Neurofibromatosis

Neurofibromatosis (NF) is a group of three conditions in which tumors grow in the nervous system.

ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Neurofibromatosis · Neurofibromatosis and Phakomatosis · See more »

Sturge–Weber syndrome

Sturge–Weber syndrome or Sturge–Weber–Krabbe disease, sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder.

ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Sturge–Weber syndrome · Phakomatosis and Sturge–Weber syndrome · See more »

Tuberous sclerosis

Tuberous sclerosis, or tuberous sclerosis complex (TSC), or epiloia (acronym of "epilepsy, low intelligence, adenoma sebaceum"), is a rare multisystem genetic disease that causes benign tumors to grow in the brain and on other vital organs such as the kidneys, heart, liver, eyes, lungs, and skin.

ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Tuberous sclerosis · Phakomatosis and Tuberous sclerosis · See more »

Von Hippel–Lindau disease

von Hippel–Lindau disease (VHL), also known as Familial cerebello retinal angiomatosis, is a rare genetic disorder with multisystem involvement.

ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Von Hippel–Lindau disease · Phakomatosis and Von Hippel–Lindau disease · See more »

The list above answers the following questions

What ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Phakomatosis have in common
What are the similarities between ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Phakomatosis

ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities and Phakomatosis Comparison

ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities has 541 relations, while Phakomatosis has 13. As they have in common 5, the Jaccard index is 0.90% = 5 / (541 + 13).

References

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