Melnick–Needles syndrome
congenital disorder that affects primarily bone development.
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Melnick–Needles syndrome
Summary
Melnick–Needles syndrome is a rare disease[1]. It draws 58 Wikipedia views per month (rare_disease category, ranking #208 of 627).[2]
Key Facts
- Melnick–Needles syndrome's instance of is recorded as rare disease[3].
- Melnick–Needles syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Melnick–Needles syndrome's instance of is recorded as class of disease[5].
- Melnick–Needles syndrome is a type of congenital disorder[6].
- Melnick–Needles syndrome is a type of otopalatodigital syndrome spectrum disorder[7].
- Melnick–Needles syndrome is a type of syndromic glaucoma[8].
- Melnick–Needles syndrome is a type of X-linked intellectual disability[9].
- Melnick–Needles syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[10].
- Melnick–Needles syndrome is a type of syndromic developmental defect of the eye[11].
- Melnick–Needles syndrome's Commons category is recorded as Melnick-Needles syndrome[12].
- Melnick–Needles syndrome's ICD-9-CM is recorded as 756.59[13].
- Melnick–Needles syndrome's genetic association is recorded as FLNA[14].
- Melnick–Needles syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2484[15].
Why It Matters
Melnick–Needles syndrome draws 58 Wikipedia views per month (rare_disease category, ranking #208 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[16] It is known by 8 alternative names across languages and contexts.[17]