Hospitals report these codes with terse, inconsistent chargemaster text. This plain-English title was written by an AI model from that text and has not been reviewed by a person, so it can be wrong. The prices on this page come straight from hospital filings and do not depend on it.
Original text from hospital filings
Molecular pathology procedure, Level 7 (eg, analysis of 11-25 exons by DNA sequence analysis, mutation scanning or duplication/deletion variants of 26-50 exons) ACADVL (acyl-CoA dehydrogenase, very long chain) (eg, very long chain acyl-coenzyme A dehydrogenase deficiency), full gene sequence ACTN4 (actinin, alpha 4) (eg, focal segmental glomerulosclerosis), full gene sequence AFG3L2 (AFG3 ATPase family gene 3-like 2 [S. cerevisiae]) (eg, spinocerebellar ataxia), full gene sequence AIRE (autoimmune regulator) (eg, autoimmune polyendocrinopathy syndrome type 1), full gene sequence ALDH7A1 (aldehyde dehydrogenase 7 family, member A1) (eg, pyridoxine-dependent epilepsy), full gene sequence ANO5 (anoctamin 5) (eg, limb-girdle muscular dystrophy), full gene sequence ANOS1 (anosmin-1) (eg, Kallmann syndrome 1), full gene sequence APP (amyloid beta [A4] precursor protein) (eg, Alzheimer disease), full gene sequence ASS1 (argininosuccinate synthase 1) (eg, citrullinemia type I), full gene sequence ATL1 (atlastin GTPase 1) (eg, spastic paraplegia), full gene sequence ATP1A2 (ATPase, Na+/K+ transporting, alpha 2 polypeptide) (eg, familial hemiplegic migraine), full gene sequence ATP7B (ATPase, Cu++ transporting, beta polypeptide) (eg, Wilson disease), full gene sequence BBS1 (Bardet-Biedl syndrome 1) (eg, Bardet-Biedl syndrome), full gene sequence BBS2 (Bardet-Biedl syndrome 2) (eg, Bardet-Biedl syndrome), full gene sequence BCKDHB (branched-chain keto acid dehydrogenase E1, beta polypeptide) (eg, maple syrup urine disease, type 1B), full gene sequence BEST1 (bestrophin 1) (eg, vitelliform macular dystrophy), full gene sequence BMPR2 (bone morphogenetic protein receptor, type II [serine/threonine kinase]) (eg, heritable pulmonary arterial hypertension), full gene sequence BRAF (B-Raf proto-oncogene, serine/threonine kinase) (eg, Noonan syndrome), full gene sequence BSCL2 (Berardinelli-Seip congenital lipodystrophy 2 [seipin]) (eg, Berardinelli-Seip congenital lipodystrophy), f
Houston, TX
See all hospitals reporting CPT 81406 →Price type
Mhhs Imaging Center’s median price of $272 is 17% below the median hospital's median price ($328), higher than 8% of the 2,046 hospitals reporting CPT 81406. The highlighted bar is where this hospital falls; shaded is the middle 50% of hospitals.
Negotiated rates from the hospital’s own file: 3 payers, 10 plan rates. A facility fee, a professional fee, a per diem and a case rate are different bills, so each is listed on its own. Open a payer to see it across hospitals.
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| # | |||||||
|---|---|---|---|---|---|---|---|
| 1 | UnitedHealthcare uhc hmo facility · case rate · outpatient | $119 | $119 | — | — | — | $119 – $119 |
| 2 | UnitedHealthcare uhc nexus facility · case rate · outpatient | $119 | $119 | — | — | — | $119 – $119 |
| 3 | UnitedHealthcare uhc ppo facility · case rate · outpatient | $119 | $119 | — | — | — | $119 – $119 |
| 4 | Healthcare Highways healthcare highways facility · case rate · outpatient | $424 | $424 | — | — | — | $424 – $424 |
| 5 | Bcbs Tx bcbs blue advantage hmo (bav) facility · case rate · outpatient | $948 | $948 | — | — | — | $948 – $948 |
| 6 | Bcbs Tx bcbs my blue health (mbh) facility · case rate · outpatient | $948 | $948 | — | — | — | $948 – $948 |
| 7 | Bcbs Tx bcbs hmo blue essentials facility · case rate · outpatient | $1.3k | $1.3k | — | — | — | $1.3k – $1.3k |
| 8 | Bcbs Tx bcbs high performance network (hpn) facility · case rate · outpatient | $1.3k | $1.3k | — | — | — | $1.3k – $1.3k |
| 9 | Bcbs Tx bcbs hmo blue premier facility · case rate · outpatient | $1.3k | $1.3k | — | — | — | $1.3k – $1.3k |
| 10 | Bcbs Tx bcbs ppo/pos facility · case rate · outpatient | $1.5k | $1.5k | — | — | — | $1.5k – $1.5k |
Last updated: Nov 6, 2024
See Molecular genetic test for very long-chain fatty acid disorder pricing across every hospital in the network reporting it, or ask Claude or any MCP client directly — see how to connect.