Table 4.

Putative Diseases or Disorders Identifiable Using GeneCards.org, HGMD, and DISEASES as Referenced Sources for the NIPA1 Gene.

Number	MalaCards ID	Name of Associated Disease	MIFTS	Solr Relevance Score
1	SPS127	Spastic Paraplegia 6, Autosomal Dominant	40	7.269
2	SPS041	Spastic Paraplegia 6	26	6.526
3	PRP016	Paraplegia	54	5.9
4	HRD010	Hereditary Spastic Paraplegia	67	5.563
5	ANG001	Angelman Syndrome	65	3.787
6	ATS013	Autosomal Recessive Congenital Ichthyosis	65	3.647
7	SPS215	Spastic Paraplegia 3, Autosomal Dominant	56	3.104
8	SPS147	Spastic Paraplegia 4, Autosomal Dominant	50	3.027
9	SPS148	Spastic Paraplegia 31, Autosomal Dominant	41	3.027
10	CMP101	Complex Hereditary Spastic Paraplegia	23	3.027
11	PRH002	Pure Hereditary Spastic Paraplegia	22	3.027
12	PRD006	Prader–Willi Syndrome	60	2.978
13	SPS107	Spastic Paraplegia 18, Autosomal Recessive	34	2.978
14	SPS099	Spastic Paraplegia 42, Autosomal Dominant	34	2.978
15	SPS021	Spastic Paraplegia 10	35	1.081
16	SCH015	Schizophrenia	76	0.187
17	ATS364	Autism	68	0.171
18	SPS057	Spasticity	38	0.171
19	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.132
20	LTR001	Lateral Sclerosis	56	0.132
21	SPS012	Spastic Paraplegia 3a	26	0.132
22	EPL164	Epilepsy	73	0.108
23	HYP595	Hypertension- Essential	87	0.076
24	BDY004	Body Mass Index Quantitative Trait Locus 11	78	0.076
25	DWN001	Down Syndrome	70	0.076
26	ATS007	Autism Spectrum Disorder	69	0.076
27	THR014	Thrombocytopenia	67	0.076
28	DYS154	Dystonia	65	0.076
29	PRP019	Peripheral Nervous System Disease	64	0.076
30	PRC016	Pre-Eclampsia	63	0.076

MalaCards InFormaTion Score (MIFTS)—annotation strength (max 100). Solr Relevance Score is generated from the Apache Lucene project by integrating, indexing, and clustering data. Source: MalaCards.org, HGMD, OMIM, ClinVar, GTR, Orphanet, DISEASES, Novoseek, and GeneCards.org.