Genetic disorders with OMIM but no gene
- Aase syndrome
- Abdallat–Davis–Farrage syndrome
- Abruzzo–Erickson syndrome
- Acrogeria
- Acropectoral syndrome
- Adams–Oliver syndrome
- Adducted thumb syndrome
- Aicardi syndrome
- Atrophodermia vermiculata
- Bazex–Dupré–Christol syndrome
- Behr syndrome
- Berdon syndrome
- Blue diaper syndrome
- Catel–Manzke syndrome
- CHIME syndrome
- Coffin–Siris syndrome
- Cronkhite–Canada syndrome
- Cutis verticis gyrata
- Diffuse panbronchiolitis
- DOOR syndrome
- Dubowitz syndrome
- Fazio–Londe disease
- Fitzsimmons–Guilbert syndrome
- Flynn–Aird syndrome
- Fountain syndrome
- Galloway Mowat syndrome
- GAPO syndrome
- Gray platelet syndrome
- Hemoglobin Lepore syndrome
- Hereditary sclerosing poikiloderma
- Howel–Evans syndrome
- Incontinentia pigmenti achromians
- Johnson–McMillin syndrome
- Kapur–Toriello syndrome
- Keratolytic winter erythema
- Laurence–Moon syndrome
- Lelis syndrome
- Lenz–Majewski syndrome
- Maffucci syndrome
- Melorheostosis
- Metaphyseal dysplasia
- Moebius syndrome
- MOMO syndrome
- Neonatal hemochromatosis
- Odonto–tricho–ungual–digital–palmar syndrome
- Ollier disease
- Paris-Trousseau syndrome
- Parry–Romberg syndrome
- Peeling skin syndrome
- Pentalogy of Cantrell
- Perlman syndrome
- Photic sneeze reflex
- Primary familial brain calcification
- Quebec platelet disorder
- Rombo syndrome
- Rud syndrome
- Scalp–ear–nipple syndrome
- Serpentine fibula-polycystic kidney syndrome
- Uncombable hair syndrome
- Urban–Rogers–Meyer syndrome
- Westerhof syndrome
- Yunis–Varon syndrome
- Zonular cataract and nystagmus
- Zori–Stalker–Williams syndrome
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Genetic disorders with OMIM but no gene
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