Neu-Laxova syndrome 2
Human disease
Press Enter · cited answer in seconds
0 sources
Summary
Neu-Laxova syndrome 2 is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- Neu-Laxova syndrome 2's instance of is recorded as rare disease[3].
- Neu-Laxova syndrome 2's instance of is recorded as class of disease[4].
- Neu-Laxova syndrome 2 is a type of serine deficiency[5].
- Neu-Laxova syndrome 2 is a type of Neu-Laxova syndrome[6].
- Neu-Laxova syndrome 2's symptoms and signs is recorded as ptosis[7].
- Neu-Laxova syndrome 2's genetic association is recorded as PSAT1[8].
- Neu-Laxova syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080075[9].
- Neu-Laxova syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0080075[10].
- Neu-Laxova syndrome 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2671[11].
- Neu-Laxova syndrome 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
Neu-Laxova syndrome 2 is known by 5 alternative names across languages and contexts.[2]