Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

55 matching diseasesClear search ×

Glanders

Equinia · Burkholderia mallei infection

ORPHA:659908

Glanzmann thrombasthenia

ORPHA:849

Glassy cell carcinoma of the cervix uteri

ORPHA:213833

Glaucoma secondary to spherophakia/ectopia lentis and megalocornea

Megalocornea-spherophakia-secondary glaucoma syndrome

ORPHA:238763

Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome

GEMSS syndrome

ORPHA:2084

Glaucoma-sleep apnea syndrome

ORPHA:2085

Glaucomatocyclitic crisis disease

Posner-Schlossman syndrome

ORPHA:636950

Diffuse lymphatic malformation

Diffuse lymphangioma · Diffuse lymphangiomatosis

ORPHA:141209

Craniosynostosis-dysmorphism-brachydactyly syndrome

Glass-Chapman-Hockley syndrome

ORPHA:1535

Osteogenesis imperfecta

Brittle bone disease · Glass bone disease

ORPHA:666

Aplasia of lacrimal and salivary glands

ALSG · Congenital absence of lacrimal puncta and salivary glands

ORPHA:86815

Benign epithelial tumor of salivary glands

ORPHA:276148

Carcinoma of esophagus, salivary gland type

Esophageal carcinoma, salivary gland type

ORPHA:418945

Cheilitis glandularis

ORPHA:1221

Congenital glaucoma

Buphthalmia · Buphthalmos

ORPHA:98976

Congenital malformation of the eye with glaucoma as a major feature

ORPHA:98631

Duplication of the pituitary gland

DPG-plus syndrome · Duplication of the pituitary gland-plus syndrome

ORPHA:314621

Dyssegmental dysplasia-glaucoma syndrome

ORPHA:1804

Familial isolated hypoparathyroidism due to agenesis of parathyroid gland

ORPHA:2239

Genetic congenital malformation of the eye with glaucoma as a major feature

ORPHA:525677

Genetic sebaceous gland anomaly

ORPHA:183460

Hearing loss-familial salivary gland insensitivity to aldosterone syndrome

Tungland-Bellman syndrome

ORPHA:3225

Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome

HELIX syndrome

ORPHA:528105

IgG4-related submandibular gland disease

Küttner tumor

ORPHA:449432

Isolated autosomal dominant hypomagnesemia, Glaudemans type

ORPHA:199326

Isolated generalized anhidrosis with normal sweat glands

ORPHA:468666

Juvenile glaucoma

ORPHA:98977

Malignant epithelial tumor of salivary glands

ORPHA:276145

Microcornea-glaucoma-absent frontal sinuses syndrome

ORPHA:2536

Multiple polyglandular tumor

ORPHA:100094

Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome

ORPHA:79118

Neovascular glaucoma

ORPHA:94058

OBSOLETE: Carcinoma of stomach, salivary gland type

OBSOLETE: Gastric carcinoma, salivary gland type

ORPHA:423781

OBSOLETE: Glaucoma associated with neural crest cell migration anomaly

ORPHA:98632

OBSOLETE: Palpebral sebaceous gland tumor

ORPHA:98585

OBSOLETE: Pleomorphic salivary gland adenoma

ORPHA:454821

OBSOLETE: Rare genetic glaucoma

ORPHA:183604

OBSOLETE: Rare glaucoma

ORPHA:98629

OBSOLETE: Secondary glaucoma due to a proliferation and differentiation anomaly

ORPHA:98637

OBSOLETE: Squamous cell carcinoma of salivary glands

ORPHA:500481

Pediatric-onset glaucoma

ORPHA:523000

Pediatric-onset glaucoma of genetic origin

Hereditary glaucoma

ORPHA:359

Primary early-onset glaucoma

ORPHA:156005

Prominent glabella-microcephaly-hypogenitalism syndrome

MacDermot-Winter syndrome

ORPHA:2083

Rare disease with glaucoma as a major feature

ORPHA:98638

Rare tumor of salivary glands

ORPHA:276142

Retinal degeneration-nanophthalmos-glaucoma syndrome

Mackay-Shek-Carr syndrome

ORPHA:1574

Salivary gland type cancer of the breast

Salivary gland type carcinoma of the breast

ORPHA:213557