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Alacrima, congenital, autosomal dominant

MedGen UID:
934803
Concept ID:
C4310836
Disease or Syndrome
Synonym: ALACRIMIA CONGENITA, AUTOSOMAL DOMINANT
 
Monarch Initiative: MONDO:0007075
OMIM®: 103420

Clinical features

From HPO
Photophobia
MedGen UID:
43220
Concept ID:
C0085636
Sign or Symptom
Excessive sensitivity to light with the sensation of discomfort or pain in the eyes due to exposure to bright light.
Lacrimal gland hypoplasia
MedGen UID:
350109
Concept ID:
C1863200
Finding
Underdevelopment of the lacrimal gland.
Lacrimal punctal atresia
MedGen UID:
354927
Concept ID:
C1863201
Congenital Abnormality
Congenital absence or closure of the opening of the lacrimal punctum.
Decreased lacrimation
MedGen UID:
116004
Concept ID:
C0235857
Finding
Abnormally decreased lacrimation, that is, reduced ability to produce tears.
Alacrima
MedGen UID:
87488
Concept ID:
C0344505
Disease or Syndrome
Absence of tear secretion.
Punctate corneal epithelial erosions
MedGen UID:
330398
Concept ID:
C1832170
Finding

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