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3-M syndrome
rare3M syndrome is a primordial growth disorder characterized by low birth weight, reduced birth length, severe postnatal growth restriction, a spectrum of minor anomalies (including facial dysmorphism) and normal intelligence.
- Identifiers
- MONDO:0007477 Orphanet:2616
- Part of
- Autosomal recessive diseaseMultiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySyndromic disease
- Also known as
- 3-MSBN · 3M syndrome · gloomy face syndrome Yakut short stature syndrome, included · Three M Syndrome · three-M slender-boned nanism
Subtypes
| Disease | Subtypes |
|---|---|
| 3M syndrome 1 | |
| 3M syndrome 2 | |
| 3M syndrome 3 |
Rare disease
Projects
Including projects on subtypes.
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