Disease Index
9,486 diseaseseyelid disease
adnexa disease that is located in the eyelid
MeSH: D005141
eyelid malformation
human disease
ICD: Q10.3
eyelid neoplasm
human disease
MeSH: D005142
eyelids malposition disorder
human disease
Fabry disease
rare human genetic lysosomal storage disorder
MeSH: D000795
Fabry Disease
Fabry disease is an X-linked lysosomal storage disorder caused by deficiency of alpha-galactosidase A enzyme, leading to accumulation of globotriaosylceramide in various tissues. Clinical manifestations include angiokeratomas, acroparesthesias, corneal opacities, cardiac and renal complications, and cerebrovascular disease. The estimated prevalence ranges from 1 in 40,000 to 1 in 117,000 live births, with variable phenotypes including classic and late-onset forms.
ICD: E75.21MeSH: D000795
FACES syndrome
human disease
MeSH: C536384
facial arteriovenous malformation
human disease
facial cleft
congenital abnormality consisting of an opening or gap in the face, which results from incomplete fusion of one or more of the embryonic facial prominences
facial dermal dysplasia type 1
facial dermoid cyst
facial diplegia with paresthesias
human disease
facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
human disease
facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation
human disease
facial dysmorphism-immunodeficiency-livedo-short stature syndrome
human disease
facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome
human disease
MeSH: C563293
facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome
MeSH: C535985
facial dysmorphism, hypertrichosis, epilepsy, intellectual and developmental delay, and gingival overgrowth syndrome
human disease
facial myokymia
human disease
facial onset sensory and motor neuronopathy
Facial Onset Sensory Motor Neuropathy syndrome
medical condition
faciocardiorenal syndrome
Faciocardiorenal syndrome is a very rare syndrome characterized by intellectual deficit, horseshoe kidney, and congenital heart defects
MeSH: C536388
facioscapulohumeral muscular dystrophy
Muscular dystrophy that classically weakens the muscles of the face (facio), shoulder girdle (scapulo) and upper arm (humerus). Weakness usually is asymmetrical and develops in other areas of the body as well, such as the abdomen and shin.
MeSH: D020391
Factor I Deficiency
medical condition
factor VII deficiency
Human disease
MeSH: D005168
factor X deficiency
Human disease
MeSH: D005171
factor XII deficiency
Human disease
MeSH: D005175
factor XIII deficiency
Human disease
ICD: D68.2MeSH: D005177
FADD-related immunodeficiency
gene (11q13.3) was found in the family and the disease is thought to follow an autosomal recessive pattern of inheritance.
failure of eruption of teeth
human disease
ICD: K00.8MeSH: C565114